Studies in Stereochemistry. XXXII. Models for 1,2-Asymmetric Induction

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1. Gunnar Ehrlich, Christian B. W. Stark. Synthesis of Cytospolide Analogues and Late-State Diversification Thereof. The Journal of Organic Chemistry 2019, 84 (6) , 3132-3147. https://doi.org/10.1021/acs.joc.8b02999
2. Gunnar Ehrlich and Christian B. W. Stark . Total Synthesis of Cytospolide D and Its Biomimetic Conversion to Cytospolides M, O, and Q. Organic Letters 2016, 18 (19) , 4802-4805. https://doi.org/10.1021/acs.orglett.6b02193
3. Salvador Pérez-Estrada, Pedro Joseph-Nathan, Hugo A. Jiménez-Vázquez, Manuel E. Medina-López, Francisco Ayala-Mata, and L. Gerardo Zepeda . Diastereoselective Preparation of (R)- and (S)-2-Methoxy-2-phenylpent-3-ynoic Acids and Their Use as Reliable Chiral Derivatizing Agents. The Journal of Organic Chemistry 2012, 77 (4) , 1640-1652. https://doi.org/10.1021/jo2016554
4. Rojita Sharma, Madhuri Manpadi, Yue Zhang, Hiyun Kim, Novruz G. Ahkmedov, and Lawrence J. Williams . Spirodiepoxide-Based Cascades: Direct Access to Diverse Motifs. Organic Letters 2011, 13 (13) , 3352-3355. https://doi.org/10.1021/ol201101e
5. Giuseppe Bartoli, Enrico Marcantoni, Mauro Marcolini, and Letizia Sambri. Applications of CeCl3 as an Environmental Friendly Promoter in Organic Chemistry. Chemical Reviews 2010, 110 (10) , 6104-6143. https://doi.org/10.1021/cr100084g
6. Albert I. Meyers. Chiral Oxazolines and Their Legacy in Asymmetric Carbon−Carbon Bond-Forming Reactions. The Journal of Organic Chemistry 2005, 70 (16) , 6137-6151. https://doi.org/10.1021/jo050470h
7. Durgesh Nadkarni,, James Hallissey, and, Carlos Mojica. Diastereoselectivity in the Reduction of α-Oxy- and α-Amino-Substituted Acyclic Ketones by Polymethylhydrosiloxane. The Journal of Organic Chemistry 2003, 68 (2) , 594-596. https://doi.org/10.1021/jo0260544
8. Michael E. Jung and, Joseph Pontillo. Synthetic Approach to Analogues of the Original Structure of Sclerophytin A. The Journal of Organic Chemistry 2002, 67 (19) , 6848-6851. https://doi.org/10.1021/jo016246j
9. Akira Otaka,, Fumihiko Katagiri,, Takayoshi Kinoshita,, Yoshihiko Odagaki,, Shinya Oishi,, Hirokazu Tamamura,, Nobuyuki Hamanaka, and, Nobutaka Fujii. Regio- and Stereoselective Synthesis of (E)-Alkene trans-Xaa-Pro Dipeptide Mimetics Utilizing Organocopper-Mediated Anti-SN2‘ Reactions. The Journal of Organic Chemistry 2002, 67 (17) , 6152-6161. https://doi.org/10.1021/jo025922u
10. Regina L. Soucy,, Denis Kozhinov, and, Victor Behar. Remarkable Diastereoselectivity in the Addition of Allylic and Unsaturated Diorganozinc Reagents to β-(N,N-Dialkylamino)-aldehydes. The Journal of Organic Chemistry 2002, 67 (6) , 1947-1952. https://doi.org/10.1021/jo016366r
11. K. S. Ravikumar,, Surajit Sinha, and, S. Chandrasekaran. Diastereoselectivity in the Reduction of Acyclic Carbonyl Compounds with Diisopropoxytitanium(III) Tetrahydroborate. The Journal of Organic Chemistry 1999, 64 (16) , 5841-5844. https://doi.org/10.1021/jo9902906
12. Goverdhan Mehta and, Jayaraman Chandrasekhar. Electronic Control of Facial Selection in Additions to Sterically Unbiased Ketones and Olefins. Chemical Reviews 1999, 99 (5) , 1437-1468. https://doi.org/10.1021/cr980369v
13. Alessandro Volonterio,, Barbara Vergani,, Marcello Crucianelli, and, Matteo Zanda, , Pierfrancesco Bravo. (R)-Trifluoro- and Difluoropyruvaldehyde N,S-Ketals:  Chiral Synthetic Equivalents of β-Trifluoro and β-Difluoro α-Amino Aldehydes. The Journal of Organic Chemistry 1998, 63 (21) , 7236-7243. https://doi.org/10.1021/jo980602p
14. Leo A. Paquette,, George D. Bennett,, Adnan Chhatriwalla, and, Methvin B. Isaac. Factors Influencing 1,4-Asymmetric Induction during Indium-Promoted Coupling of Oxygen-Substituted Allylic Bromides to Aldehydes in Aqueous Solution. The Journal of Organic Chemistry 1997, 62 (10) , 3370-3374. https://doi.org/10.1021/jo970158a
15. Leo A. Paquette and, Thomas M. Mitzel. Addition of Allylindium Reagents to Aldehydes Substituted at Cα or Cβ with Heteroatomic Functional Groups. Analysis of the Modulation in Diastereoselectivity Attainable in Aqueous, Organic, and Mixed Solvent Systems. Journal of the American Chemical Society 1996, 118 (8) , 1931-1937. https://doi.org/10.1021/ja953682c
16. David B. Collum. Is N,N,N',N'-tetramethylethylenediamine a good ligand for lithium?. Accounts of Chemical Research 1992, 25 (10) , 448-454. https://doi.org/10.1021/ar00022a003
17. Edward R. Biehl and Subhash P. Khanapure. Synthesis of polycyclics via aryne arylation reactions. Accounts of Chemical Research 1989, 22 (8) , 275-281. https://doi.org/10.1021/ar00164a003
18. John M. Brown. The Historical Development of Asymmetric Hydrogenation. 2021,,, 1-24. https://doi.org/10.1002/9783527822294.ch1
19. Dipak K. Mandal. Ionic reactions 2: Diastereoselectivity and asymmetric synthesis. 2021,,, 303-374. https://doi.org/10.1016/B978-0-12-824092-2.00007-1
20. Johannes M. Wiest, Michael L. Conner, M. Kevin Brown. Synthesis of (−)-Hebelophyllene E: An Entry to Geminal Dimethyl-Cyclobutanes by [2+2] Cycloaddition of Alkenes and Allenoates. Angewandte Chemie 2018, 130 (17) , 4737-4741. https://doi.org/10.1002/ange.201801110
21. Johannes M. Wiest, Michael L. Conner, M. Kevin Brown. Synthesis of (−)-Hebelophyllene E: An Entry to Geminal Dimethyl-Cyclobutanes by [2+2] Cycloaddition of Alkenes and Allenoates. Angewandte Chemie International Edition 2018, 57 (17) , 4647-4651. https://doi.org/10.1002/anie.201801110
22. Hua Wu, Qian Wang, Jieping Zhu. Organocatalytic Enantioselective Acyloin Rearrangement of α-Hydroxy Acetals to α-Alkoxy Ketones. Angewandte Chemie 2017, 129 (21) , 5952-5955. https://doi.org/10.1002/ange.201701098
23. Hua Wu, Qian Wang, Jieping Zhu. Organocatalytic Enantioselective Acyloin Rearrangement of α-Hydroxy Acetals to α-Alkoxy Ketones. Angewandte Chemie International Edition 2017, 56 (21) , 5858-5861. https://doi.org/10.1002/anie.201701098
24. Tianlei Li, Abdellatif Tikad, Maxime Durka, Weidong Pan, Stéphane P. Vincent. Multigram-scale synthesis of l,d-heptoside using a Fleming-Tamao oxidation promoted by mercuric trifluoroacetate. Carbohydrate Research 2016, 432 , 71-75. https://doi.org/10.1016/j.carres.2016.07.010
25. Sunil Kumar Talapatra, Bani Talapatra. Fundamental Stereochemical Concepts and Nomenclatures. 2015,,, 23-201. https://doi.org/10.1007/978-3-642-45410-3_2
26. D.M. Huryn. 1.01 Carbanions of Alkali and Alkaline-Earth Cations: (II) Selectivity of Carbonyl Addition Reactions. 2014,,, 1-26. https://doi.org/10.1016/B978-0-08-097742-3.00102-6
27. Long-Shiang Li, Duen-Ren Hou. Diastereoselective vinylalumination for the synthesis of pericosine A, B and C. RSC Adv. 2014, 4 (1) , 91-97. https://doi.org/10.1039/C3RA45871G
28. Peter H Huy, Julia C Westphal, Ari M P Koskinen. Concise, stereodivergent and highly stereoselective synthesis of cis- and trans -2-substituted 3-hydroxypiperidines – development of a phosphite-driven cyclodehydration. Beilstein Journal of Organic Chemistry 2014, 10 , 369-383. https://doi.org/10.3762/bjoc.10.35
29. Abdellatif Tikad, Stéphane P. Vincent. Synthetic Methodologies toward Aldoheptoses and Their Applications to the Synthesis of Biochemical Probes and LPS Fragments. 2013,,, 29-65. https://doi.org/10.1002/9783527658947.ch2
30. Scott G. Nelson, Robert D. Dura, Timothy J. Peelen. Catalytic Asymmetric Ketene [2 + 2] and [4 + 2] Cycloadditions. 2012,,, 471-621. https://doi.org/10.1002/0471264180.or082.02
31. M. Braun. 2.12 Selected Diastereoselective Reactions: Additions of Achiral Carbanions to Chiral Aldehydes and Ketones. 2012,,, 346-369. https://doi.org/10.1016/B978-0-08-095167-6.00207-X
32. . Cram's Rule. 2010,,, 756-760. https://doi.org/10.1002/9780470638859.conrr167
33. Xin-Gang Xie, Xun-Wei Wu, Hing-Ken Lee, Xiao-Shui Peng, Henry N. C. Wong. Total Synthesis of Plakortone B. Chemistry - A European Journal 2010, 16 (23) , 6933-6941. https://doi.org/10.1002/chem.201000189
34. Manfred Braun. Lithium Carbenoids. 2009,,https://doi.org/10.1002/9780470682531.pat0309
35. Koichi Narita, Takuya Kikuchi, Kazuhiro Watanabe, Toshiya Takizawa, Takamasa Oguchi, Kyosuke Kudo, Keisuke Matsuhara, Hideki Abe, Takao Yamori, Minoru Yoshida, Tadashi Katoh. Total Synthesis of the Bicyclic Depsipeptide HDAC Inhibitors Spiruchostatins A and B, 5′′- epi -Spiruchostatin B, FK228 (FR901228) and Preliminary Evaluation of Their Biological Activity. Chemistry - A European Journal 2009, 15 (42) , 11174-11186. https://doi.org/10.1002/chem.200901552
36. Dibakar Goswami, Angshuman Chattopadhyay, Subrata Chattopadhyay. Metal-dependent modulation of diastereoselectivity in the Barbier-type crotylation of (R)-cyclohexylideneglyceraldehyde. Tetrahedron: Asymmetry 2009, 20 (17) , 1957-1961. https://doi.org/10.1016/j.tetasy.2009.08.013
37. J. Y. Yuan, X. C. Liao, H. M. Wang, M. S. Tang. Camphor-based α-bromoketones for the asymmetric darzens reaction: Insights into the mechanism using density functional theory. Journal of Structural Chemistry 2008, 49 (5) , 818-827. https://doi.org/10.1007/s10947-008-0144-y
38. Yasumitsu Suzuki, Daisuke Kaneno, Masaya Miura, Shuji Tomoda. Solvent effects on the diastereoselection in LiAlH4 reduction of α-substituted ketones. Tetrahedron Letters 2008, 49 (27) , 4223-4226. https://doi.org/10.1016/j.tetlet.2008.05.002
39. . References. 2007,,, 315-356. https://doi.org/10.1002/9783527615698.refs
40. James McNulty, Jerald J. Nair, Marcin Sliwinski, Laura E. Harrington, Siyaram Pandey. Unusual Magnesium Chloride Catalyzed Non-Evansanti-Aldol Reactions of an EnolizableL-Threose Derivative. European Journal of Organic Chemistry 2007, 2007 (34) , 5669-5673. https://doi.org/10.1002/ejoc.200700854
41. Kuheli Chakrabarty, Sukhendu Roy, Gourab Kanti Das, Nityagopal Mondal. Pi-diastereofacial selectivity on carbonyl enophile in carbonyl ene reaction: A new insight on the substituent effect in ene cyclization. Journal of Molecular Structure: THEOCHEM 2007, 805 (1-3) , 1-7. https://doi.org/10.1016/j.theochem.2006.10.016
42. D. A. Evans, J. V. Nelson, T. R. Taber. Stereoselective Aldol Condensations. 2007,,, 1-115. https://doi.org/10.1002/9780470147221.ch1
43. Vito Convertino, Peter Manini, W. Bernd Schweizer, François Diederich. First asymmetric synthesis of a differentially silyl-protected tris(alkynyl)methyl methyl ether. Organic & Biomolecular Chemistry 2006, 4 (7) , 1206. https://doi.org/10.1039/b601380e
44. Yonghua Zhao, Nan Jiang, Shufeng Chen, Cheng Peng, Xiaomei Zhang, Yaping Zou, Shiwei Zhang, Jianbo Wang. Concise and diastereoselective approach to syn- and anti-N-tosyl-α-hydroxy β-amino acid derivatives. Tetrahedron 2005, 61 (27) , 6546-6552. https://doi.org/10.1016/j.tet.2005.04.054
45. Michael Larsson, Elodie Galandrin, Hans-Erik Högberg. Diastereoselective addition of organozinc reagents to 2-alkyl-3-(arylsulfanyl)propanals. Tetrahedron 2004, 60 (47) , 10659-10669. https://doi.org/10.1016/j.tet.2004.09.005
46. Dieter Schinzer. Silicon in Organic Synthesis: Selective Transformations with Pentacoordinate Silicon Compounds. 2003,,, 123-127. https://doi.org/10.1002/9783527620784.ch14a
47. Dorota Gryko, Joanna Cha?ko, Janusz Jurczak. Synthesis and reactivity ofN-protected-?-amino aldehydes. Chirality 2003, 15 (6) , 514-541. https://doi.org/10.1002/chir.10243
48. Ahmed I Khodair, Richard R Schmidt. Synthesis of C-glycosyl compounds of N-acetylneuraminic acid from d-gluconolactone. Carbohydrate Research 2002, 337 (21-23) , 1967-1978. https://doi.org/10.1016/S0008-6215(02)00176-3
49. Yasuhisa Senda. Role of the heteroatom on stereoselectivity in the complex metal hydride reduction of six-membered cyclic ketones. Chirality 2002, 14 (2-3) , 110-120. https://doi.org/10.1002/chir.10051
50. Michael Larsson, Hans-Erik Högberg. Diastereoselective addition of methylmetal reagents to 2-methylaldehydes. Tetrahedron 2001, 57 (35) , 7541-7548. https://doi.org/10.1016/S0040-4020(01)00713-X
51. Alessandro Volonterio, Pierfrancesco Bravo, Eleonora Corradi, Giovanni Fronza, Stefano V Meille, Barbara Vergani, Matteo Zanda. Unusual nonchelation controlled allylation of a N -monoprotected α-amino aldehyde: stereoselective entry to nonracemic trifluoromethyl dipeptide isosteres. Journal of Fluorine Chemistry 2001, 108 (2) , 245-252. https://doi.org/10.1016/S0022-1139(01)00363-3
52. Woo Song Lee, Kyu-Tae Chang, Ki Chang Jang, Ho-Yong Park, Young-Kook Kim, Ki Hun Park. Diastereoselective Iodoamidation of 3-Acetoxybut-1-enylamines: Synthesis of 3-Acetoxy-4-iodo-2-(p-methoxybenzyl)pyrrolidines. HETEROCYCLES 2001, 55 (6) , 1173. https://doi.org/10.3987/COM-01-9206
53. Yoshihide Usami, Takashi Ikura, Taro Amagata, Atsushi Numata. First total syntheses and configurational assignments of cytotoxic trichodenones A–C. Tetrahedron: Asymmetry 2000, 11 (18) , 3711-3725. https://doi.org/10.1016/S0957-4166(00)00329-3
54. Alberto Avenoza, Carlos Cativiela, Francisco Corzana, Jesús M Peregrina, Marı́a M Zurbano. Asymmetric synthesis of all isomers of α-methyl-β-phenylserine. Tetrahedron: Asymmetry 2000, 11 (10) , 2195-2204. https://doi.org/10.1016/S0957-4166(00)00149-X
55. Yukiyasu Chounan, Yasuo Ono, Shinji Nishii, Haruo Kitahara, Shoei Ito, Yoshinori Yamamoto. 1,2-Asymmetric Induction in the Conjugate Addition of Organocopper Reagents to γ-Aryl α,β-Unsaturated Carbonyl Derivatives. Tetrahedron 2000, 56 (18) , 2821-2831. https://doi.org/10.1016/S0040-4020(00)00137-X
56. Jan Marcus, Guido W.M Vandermeulen, Johannes Brussee, Arne van der Gen. Diastereoselective addition of HCN to Garner's aldehyde. Tetrahedron: Asymmetry 1999, 10 (8) , 1617-1622. https://doi.org/10.1016/S0957-4166(99)00159-7
57. Jacqueline C. Bussolari, Kimberly Beers, Praful Lalan, William V. Murray, Diane Gauthier, Patricia McDonnell. Addition of Acrylamide to Amino Aldehydes to Generate Non-Baylis-Hillman Adducts. Formation of Novel N-Acylhemiaminals. Chemistry Letters 1998, 27 (8) , 787-788. https://doi.org/10.1246/cl.1998.787
58. Manfred Braun. 1-Alkenyllithium-Reagentien mit einem Heteroatomsubstituenten in derα-Position: Carbanionen und Carbenoide zur C-C-Verknüpfung. Angewandte Chemie 1998, 110 (4) , 444-465. https://doi.org/10.1002/(SICI)1521-3757(19980216)110:4<444::AID-ANGE444>3.0.CO;2-J
59. Dorota Gryko, Zofia Urbańczyk-Lipkowska, Janusz Jurczak. Diastereoselective addition of vinylmagnesium halides to variously N-mono- and N,N-diprotected l-alaninals. Tetrahedron: Asymmetry 1997, 8 (24) , 4059-4067. https://doi.org/10.1016/S0957-4166(97)00558-2
60. Dorota Gryko, Zofia Urbańczyk-Lipkowska, Janusz Jurczak. Diastereoselective addition of allyl reagents to. Tetrahedron 1997, 53 (39) , 13373-13382. https://doi.org/10.1016/S0040-4020(97)00850-8
61. Henryk Gruza, Krzysztof Kiciak, Antoni Krasiński, Janusz Jurczak. The highly diastereocontrolled addition of the lithium derivative of tert-butyldimethylsilyl propargyl ether to. Tetrahedron: Asymmetry 1997, 8 (15) , 2627-2631. https://doi.org/10.1016/S0957-4166(97)00306-6
62. Kimiko Kobayashi, Takayuki Kato, Masafumi Unno, Shinji Masuda. Asymmetric Synthesis of Organosilicon Compounds Using a C 2 Chiral Auxiliary. Bulletin of the Chemical Society of Japan 1997, 70 (6) , 1393-1401. https://doi.org/10.1246/bcsj.70.1393
63. Stefan Oscarson. Synthesis of oligosaccharides of bacterial origin containing heptoses, uronic acids and fructofuranoses as synthetic challenges. 1997,,, 171-202. https://doi.org/10.1007/BFb0119223
64. Yoshiki Morimoto, Atsushi Mikami, Shin-itsu Kuwabe, Haruhisa Shirahama. Stereocontrolled synthesis of C10-C22 fragment of the immunosuppressant FK 506. An occurrence of complementary stereoselectivity in the C15 ketone reduction. Tetrahedron: Asymmetry 1996, 7 (12) , 3371-3390. https://doi.org/10.1016/S0957-4166(96)00445-4
65. Jean-Philippe Surivet, Jacques Goré, Jean-Michel Vatèle. Enantioselective synthesis of (+)-goniodiol and of its naturally occurring acetylated analogs. Tetrahedron 1996, 52 (47) , 14877-14890. https://doi.org/10.1016/0040-4020(96)00918-0
66. Michèle Gerster, Kurt Schenk, Philippe Renaud. Stereoselektivität in Reaktionen von 1, 2-Dioxysubstituierten Radikalen unter Chelatkontrolle: ein unerwartetes Resultat. Angewandte Chemie 1996, 108 (20) , 2523-2525. https://doi.org/10.1002/ange.19961082019
67. Mugio Nishizawa, Hidetoshi Yamada. Intensely Sweet Saponin Osladin: Synthetic and Structural Study. 1996,,, 25-36. https://doi.org/10.1007/978-1-4613-0413-5_3
68. Alessandro Dondoni, Pedro Merino. Thiazoles. 1996,,, 373-474. https://doi.org/10.1016/B978-008096518-5.00064-2
69. . Volume 3 References. 1996,,, 817-932. https://doi.org/10.1016/B978-008096518-5.00249-5
70. Manfred Braun, Hellmut Mahler. Non-chelate-controlled addition of 1-Bromo-1-lithio-1-alkenes toO-protected lactaldehydes and 3-alkoxybutyraldehydes. Liebigs Annalen 1995, 1995 (1) , 29-40. https://doi.org/10.1002/jlac.199519950107
71. Teruaki Mukaiyama, Shū Kobayashi. Tin(II) Enolates in the Aldol, Michael, and Related Reactions. 1994,,, 1-103. https://doi.org/10.1002/0471264180.or046.01
72. G. Santer, K. H. Ongania. Synthese von benzanellierten Carbacephamen, 1. Mitt.. Monatshefte für Chemie - Chemical Monthly 1994, 125 (1) , 71-78. https://doi.org/10.1007/BF00811676
73. Gaetano Barbaro, Arturo Battaglia, Patrizia Giorgianni, Daria Giacomini. Cyclocondensation reactions of optically active α-alkoxy aldehydes to ketene imines: Synthesis of chiral 2-iminooxetanes. Tetrahedron 1993, 49 (20) , 4293-4306. https://doi.org/10.1016/S0040-4020(01)85745-8
74. Robert J.P. Corriu, Gérard F. Lanneau, Zhifang Yu. Intramolecular nucleophilic catalysis. Stereoselective hydrosilylation of diketones and α-hydroxyketones.. Tetrahedron 1993, 49 (40) , 9019-9030. https://doi.org/10.1016/S0040-4020(01)91219-0
75. G. J. P. H. Boons, M. Overhand, G. A. van der Marel, J. H. van Boom. Synthesis of two branched heptopyranoside- (L,D-Hepp)-containing trisaccharides of the inner-core region of Citrobacter PCM 1487. Recueil des Travaux Chimiques des Pays-Bas 1992, 111 (3) , 144-148. https://doi.org/10.1002/recl.19921110306
76. Masahiko Isaka, Satoshi Ejiri, Eiichi Nakamura. General synthesis of cyclopropenones and their acetals. Tetrahedron 1992, 48 (11) , 2045-2057. https://doi.org/10.1016/S0040-4020(01)88873-6
77. David J. Ager, Michael B. East. Methodology to establish 1,2- and 1,3-difunctionality for the synthesis of carbohydrate derivates. Tetrahedron 1992, 48 (14) , 2803-2894. https://doi.org/10.1016/S0040-4020(01)90970-6
78. Thavrin Manickum, Gregory Roos. Stereoselective Addition of Methyl Acrylate to α-Amino Aldehydes. Synthetic Communications 1991, 21 (22) , 2269-2274. https://doi.org/10.1080/00397919108021585
79. Yoshiki Morimoto, Atsushi Mikami, Shin-itsu Kuwabe, Haruhisa Shirahama. A synthesis of C1–C22 fragment of the immunosuppressant FK 506. Stereoselective construction of (E)-trisubstituted double bond (C19–C20) via ester-enolate claisen rearrangement. Tetrahedron Letters 1991, 32 (25) , 2909-2912. https://doi.org/10.1016/0040-4039(91)80646-N
80. Donna M. Huryn. Carbanions of Alkali and Alkaline Earth Cations: (ii) Selectivity of Carbonyl Addition Reactions. 1991,,, 49-75. https://doi.org/10.1016/B978-0-08-052349-1.00002-0
81. Jan Epsztajn, Andrzej Jóźwiak, Krzysztof Czech, Aleksandra K. Szcześniak. Application of organolithium and related reagents in synthesis, part VI. A general study of the lithiation of secondary picoline- and isonicotine amides. Monatshefte für Chemie Chemical Monthly 1990, 121 (11) , 909-921. https://doi.org/10.1007/BF00808955
82. J. Epsztajn, A. Jóźwiak, A. K. Szcześniak. Application of Organolithium and Related Reagents in Synthesis, Part 8. Synthesis of 3-Benzylpicolinic and 3-Benzylisonicotinic Acids. Synthetic Communications 1990, 20 (17) , 2623-2629. https://doi.org/10.1080/00397919008051470
83. Pierre Vogel. Synthesis of Rare Carbohydrates and Biomolecules from Furan. Bulletin des Sociétés Chimiques Belges 1990, 99 (6) , 395-439. https://doi.org/10.1002/bscb.19900990606
84. Michel Gomis, B. Serge Kirkiacharian. Reductions par les hydrures et hydroboration etude de la stereoselectivite de nouvelles voies d'acces aux 3-arylmethyl-4-chromanols (Homoisoflavanols). Tetrahedron 1990, 46 (6) , 1849-1858. https://doi.org/10.1016/S0040-4020(01)89754-4
85. Shailaja Shirodkar, Maryellen Nerz-Stormes, Edward R. Thornton. Asymmetric aldol reactions. Mechanism of solvent effect on stereoselectivity is specific, stoichiometric binding of tetrahydrofuran to a chiral titanium enolate. Tetrahedron Letters 1990, 31 (33) , 4699-4702. https://doi.org/10.1016/S0040-4039(00)97710-4
86. Mohamed Dasser, Françoise Chrétien, Yves Chapleur. A facile and stereospecific synthesis of L -glycerol- D -manno-heptose and some derivatives. J. Chem. Soc., Perkin Trans. 1 1990, 42 (11) , 3091-3094. https://doi.org/10.1039/P19900003091
87. Manfred Braun, Hellmut Mahler. Nicht-chelatkontrollierte Additionen von 1-Brom-1-lithio-1-alkenen anO-geschützte Lactaldehyde. Angewandte Chemie 1989, 101 (7) , 948-950. https://doi.org/10.1002/ange.19891010723
88. D. Schinzer. Selektive Transformationen mit pentakoordinierten Siliciumverbindungen. Nachrichten aus Chemie, Technik und Laboratorium 1989, 37 (1) , 28-30. https://doi.org/10.1002/nadc.19890370110
89. E. O. M. Orlemans, W. Verboom, B. H. M. Lammerink, D. N. Reinhoudt. α-Amino ketones derived from L-proline, as precursors for isomitosanes and mitosenes. Recueil des Travaux Chimiques des Pays-Bas 1989, 108 (2) , 64-72. https://doi.org/10.1002/recl.19891080206
90. Jan Epsztajn, Adam Bieniek, Mieczysław W. Płotka, Krzysztof Suwald. Application of organolithium and related reagents in synthesis. Part 7. Synthesis and metallion of 4-methoxypicolin- and 2-methoxyisonicotin-anilides. A useful method for preparation of 2, 3, 4-trisubstituted pyridines. Tetrahedron 1989, 45 (23) , 7469-7476. https://doi.org/10.1016/S0040-4020(01)89209-7
91. Sławomir Jarosz. Stereoselective reduction of higher sugar enones with zinc borohydride. Carbohydrate Research 1988, 183 (2) , 201-207. https://doi.org/10.1016/0008-6215(88)84074-6
92. Dieter Seebach, Geo Adam, Thomas Gees, Martin Schiess, Wolfgang Weigand. Scope and limitations of the TiCl4-mediated additions of isocyanides to aldehydes and ketones with formation of α-hydroxycarboxylic acid amides. Chemische Berichte 1988, 121 (3) , 507-517. https://doi.org/10.1002/cber.19881210319
93. B. Fraser-Reid, R. Mootoo, V. Date, S. Handa. Novel Carbohydrate Transformations Discovered en Route to Natural Products. 1988,,, 89-106. https://doi.org/10.1007/978-3-642-74017-6_5
94. George Just, Brian O'Connor. Synthesis of the 5R, 8R, 9S, 11R dephosphorylated derivative of CI-920, a novel antitumor agent.. Tetrahedron Letters 1988, 29 (7) , 753-756. https://doi.org/10.1016/S0040-4039(00)80201-4
95. Lori Crenshaw, Subhash P. Khanapure, Upali Siriwardane, Edward R. Biehl. A stereocontrolled synthesis of cis-3,4-diarylisochroman-1-ones through diastereoselective reaction of benzaldehydes and α-lithio-2-cyanodiarylmethane intermediates.. Tetrahedron Letters 1988, 29 (31) , 3777-3780. https://doi.org/10.1016/S0040-4039(00)82112-7
96. Makoto Fujita, Haruhito Oishi, Tamejiro Hiyama. REDUCTION OF OXIMES WITH HYDROSILANE/H + REAGENT. Chemistry Letters 1986, 15 (5) , 837-838. https://doi.org/10.1246/cl.1986.837
97. H.K. Müller, L. Keil, W. Gerhard. Enantiomere der 2,2'-dinitrobiphenyl-6,6'- dicarbonsäure als stereoselektiv wirksame, reversible schutzgruppen-I. Tetrahedron 1986, 42 (5) , 1529-1532. https://doi.org/10.1016/S0040-4020(01)87372-5
98. Janusz Jurczak, Stanislaw Pikul, Tomasz Bauer. Tetrahedron report number 195 (R)- and (S)-2,3-0-isopropylideneglyceraldehyde in stereoselective organic synthesis. Tetrahedron 1986, 42 (2) , 447-488. https://doi.org/10.1016/S0040-4020(01)87445-7
99. Janusz Jurczak, Tomasz Bauer. Stereochemistry of diels-alder reaction at high-pressure: influence of pressure on asymmetric induction in (4+2)cycloaddition of 1-methoxybuta-1,3-diene to 2,3-o-isopropylidene-D-glyceraldehyde. Tetrahedron 1986, 42 (18) , 5045-5052. https://doi.org/10.1016/S0040-4020(01)88056-X
100. Janusz Jurczak, Tommasz Bauer, Sławomir Jarosz. Stereochemistry of diels-alder reaction at high pressure: asymmetric induction in the reaction of 1-methoxybuta-1,3-diene with sugar aldehydes. Tetrahedron 1986, 42 (23) , 6477-6486. https://doi.org/10.1016/S0040-4020(01)88110-2