Reactions of Isopropenyl AcetateClick to copy article linkArticle link copied!
Note: In lieu of an abstract, this is the article's first page.
Cited By
This article is cited by 109 publications.
- Davide Rigo, Daniele Polidoro, Lorenzo Marcuzzo, Alvise Perosa, Maurizio Selva. Isopropenyl Acetate for the Continuous-Flow Synthesis of Triacetin, Solketal Acetate, and Allyl Acetate from Pure or Crude Glycerol. ACS Sustainable Chemistry & Engineering 2023, 11
(34)
, 12602-12613. https://doi.org/10.1021/acssuschemeng.3c02197
- Irina Geibel, Anna Dierks, Marc Schmidtmann, and Jens Christoffers . Formation of δ-Lactones by Cerium-Catalyzed, Baeyer–Villiger-Type Coupling of β-Oxoesters, Enol Acetates, and Dioxygen. The Journal of Organic Chemistry 2016, 81
(17)
, 7790-7798. https://doi.org/10.1021/acs.joc.6b01441
- Yinchun Jiao, Chenzhong Cao, and Zaichun Zhou . Direct Synthesis of anti-1,3-Diols through Nonclassical Reaction of Aryl Grignard Reagents with Isopropenyl Acetate. Organic Letters 2011, 13
(2)
, 180-183. https://doi.org/10.1021/ol102520y
- Wei Cui, Jiawen Zhu, Wangcai Liu, Bin Wu and Kui Chen. Isobaric Vapor−Liquid Equilibria for the Binary Systems of Acetic Acid + Isopropenyl Acetate, Acetic Acid + Acetylacetone, and Water + Acetylacetone. Journal of Chemical & Engineering Data 2009, 54
(2)
, 318-322. https://doi.org/10.1021/je800345j
- Wei Cui, Jiawen Zhu, Wangcai Liu, Bin Wu and Kui Chen. Isobaric Vapor–Liquid Equilibria for Binary Systems of Acetone + Isopropenyl Acetate, 2-Butanone + Isopropenyl Acetate, and Isopropenyl Acetate + Acetylacetone at 101.3 kPa. Journal of Chemical & Engineering Data 2008, 53
(2)
, 503-507. https://doi.org/10.1021/je700605t
- Chien-Tien Chen,, Jen-Huang Kuo,, Cheng-Hsiu Ku,, Shiue-Shien Weng, and, Cheng-Yuan Liu. Nucleophilic Acyl Substitutions of Esters with Protic Nucleophiles Mediated by Amphoteric, Oxotitanium, and Vanadyl Species. The Journal of Organic Chemistry 2005, 70
(4)
, 1328-1339. https://doi.org/10.1021/jo0484878
- Palanichamy Ilankumaran and, John G. Verkade. Highly Selective Acylation of Alcohols Using Enol Esters Catalyzed by Iminophosphoranes. The Journal of Organic Chemistry 1999, 64
(25)
, 9063-9066. https://doi.org/10.1021/jo990928d
- Akihiro Orita,, Akihiro Mitsutome, and, Junzo Otera. Distannoxane-Catalyzed Highly Selective Acylation of Alcohols. The Journal of Organic Chemistry 1998, 63
(8)
, 2420-2421. https://doi.org/10.1021/jo9800412
- Alexander V. Aksenov, Dinara C. Makieva, Rodion A. Arestov, Nikolai A. Arutiunov, Dmitrii A. Aksenov, Nicolai A. Aksenov, Alexander V. Leontiev, Inna V. Aksenova. Metal-Free, PPA-Mediated Fisher Indole Synthesis via Tandem Hydroamination–Cyclization Reaction between Simple Alkynes and Arylhydrazines. International Journal of Molecular Sciences 2024, 25
(16)
, 8750. https://doi.org/10.3390/ijms25168750
- Davide Rigo, Anthony F. Masters, Thomas Maschmeyer, Maurizio Selva, Giulia Fiorani. Isopropenyl Esters (iPEs) in Green Organic Synthesis. Chemistry – A European Journal 2022, 28
(40)
https://doi.org/10.1002/chem.202200431
- Davide Di Francesco, Davide Rigo, Kiran Reddy Baddigam, Aji P. Mathew, Niklas Hedin, Maurizio Selva, Joseph S. M. Samec. A New Family of Renewable Thermosets: Kraft Lignin Poly‐adipates. ChemSusChem 2022, 15
(11)
https://doi.org/10.1002/cssc.202200326
- Jean‐Marico Speldrich, Jens Christoffers. Mechanistic Insights into the Formation of δ‐Lactones by Cerium‐Catalyzed Aerobic Coupling of β‐Oxoesters with Enol Acetates. European Journal of Organic Chemistry 2021, 2021
(6)
, 907-914. https://doi.org/10.1002/ejoc.202001532
- Davide Rigo, Roberto Calmanti, Alvise Perosa, Maurizio Selva. A transesterification–acetalization catalytic tandem process for the functionalization of glycerol: the pivotal role of isopropenyl acetate. Green Chemistry 2020, 22
(16)
, 5487-5496. https://doi.org/10.1039/D0GC01775B
- Richard C. Larock, Anton V. Dubrovskiy, Nataliya A. Markina. Alkylation and Acylation of Aldehydes, Ketones, and Their Derivatives. 2018, 1-145. https://doi.org/10.1002/9781118662083.cot08-013
- Richard C. Larock, Roman Rozhkov. Inverconversion of Nitriles, Carboxylic Acids, and Derivatives. 2018, 1-81. https://doi.org/10.1002/9781118662083.cot09-009
- Xiaotao Zhu, Bo Qian, Rongbiao Wei, Jian-Dong Huang, Hongli Bao. Protection of COOH and OH groups in acid, base and salt free reactions. Green Chemistry 2018, 20
(7)
, 1444-1447. https://doi.org/10.1039/C8GC00037A
- Andrea Temperini, Lucio Minuti, Tommaso Morini, Ornelio Rosati, Francesca Piazzolla. Isopropenyl acetate: A cheap and general acylating agent of alcohols under metal-free conditions. Tetrahedron Letters 2017, 58
(43)
, 4051-4053. https://doi.org/10.1016/j.tetlet.2017.09.007
- Irina Geibel, Anna Dierks, Thomas Müller, Jens Christoffers. Formation of δ‐Lactones with
anti
‐Baeyer–Villiger Regiochemistry: Investigations into the Mechanism of the Cerium‐Catalyzed Aerobic Coupling of β‐Oxoesters with Enol Acetates. Chemistry – A European Journal 2017, 23
(30)
, 7245-7254. https://doi.org/10.1002/chem.201605468
- Amita Sharma, Santosh Kumar Giri, K. P. Ravindranathan Kartha, Rajender S. Sangwan. Value-additive utilization of agro-biomass: preparation of cellulose triacetate directly from rice straw as well as other cellulosic materials. RSC Advances 2017, 7
(21)
, 12745-12752. https://doi.org/10.1039/C7RA00078B
- Shengzong Liang, Gerald B. Hammond, Bo Xu. Efficient hydration of alkynes through acid-assisted Brønsted acid catalysis. Chemical Communications 2015, 51
(5)
, 903-906. https://doi.org/10.1039/C4CC08938C
- Maisa Bushra, Xiao‐Yun Xu, Si‐Yi Pan. Microwave assisted acetylation of mung bean starch and the catalytic activity of potassium carbonate in free‐solvent reaction. Starch - Stärke 2013, 65
(3-4)
, 236-243. https://doi.org/10.1002/star.201200081
- Zihan Wang, Bin Wu, Jiawen Zhu, Kui Chen, Zhuoran Zhang. Liquid–liquid equilibrium for the ternary system isopropenyl acetate+water+acetic acid at 298.2K, 313.2K, 323.2K and 333.2K. Fluid Phase Equilibria 2011, 311 , 54-58. https://doi.org/10.1016/j.fluid.2011.09.001
- Harold E. Zaugg. β‐Lactones. 2011, 305-363. https://doi.org/10.1002/0471264180.or008.07
- Shiue-Shien Weng, Chih-Shueh Ke, Fong-Kuang Chen, You-Fu Lyu, Guan-Ying Lin. Transesterification catalyzed by iron(III) β-diketonate species. Tetrahedron 2011, 67
(9)
, 1640-1648. https://doi.org/10.1016/j.tet.2011.01.009
- Christoph Taeschler. Ketenes, Ketene Dimers, and Related Substances. 2010, 1-54. https://doi.org/10.1002/0471238961.1105200501020105.a01.pub2
- Valérie Salinier, Gerald P. Niccolai, Véronique Dufaud, Jean‐Marie Basset. Silica‐Supported Zirconium Complexes and their Polyoligosilsesquioxane Analogues in the Transesterification of Acrylates: Part 2. Activity, Recycling and Regeneration. Advanced Synthesis & Catalysis 2009, 351
(13)
, 2168-2177. https://doi.org/10.1002/adsc.200900274
- Yuhya Watanabe, Tohru Sakakibara. Synthesis of methyl 4,6-O-benzylidene-2,3-dideoxy-5-thio-β-dl-threo-hex-2-enopyranoside via hetero-Diels–Alder reaction and unusual stabilities of 1,5-anhydro-4,6-O-benzylidene 2,3-dideoxy-5-thio-dl-threo-hex-2-enitol. Tetrahedron 2009, 65
(3)
, 599-606. https://doi.org/10.1016/j.tet.2008.11.025
- Andrew J. Carpenter, Robert S. Coleman, Xuejun Zhang, Richard P. Hsung. 1-Acetoxy-1,3-butadiene. 2007https://doi.org/10.1002/9780470842898.ra021.pub2
- Mohamed Jebrane, Gilles Sèbe. A novel simple route to wood acetylation by transesterification with vinyl acetate. Holzforschung 2007, 61
(2)
, 143-147. https://doi.org/10.1515/HF.2007.026
- Tse‐Lok Ho, Mary Fieser, Louis Fieser. 1‐Acetoxy‐1,3‐butadiene. 2006https://doi.org/10.1002/9780471264194.fos00086
- Tse‐Lok Ho, Mary Fieser, Louis Fieser. Isopropenyl acetate. 2006https://doi.org/10.1002/9780471264194.fos06020
- O. Yu. Krasnoslobodtseva, F. A. Valeev, O. V. Shitikova, G. A. Tolstikov. Inhibition of intramolecular reactions of (+)-δ-cadinol. Russian Journal of Organic Chemistry 2006, 42
(9)
, 1321-1324. https://doi.org/10.1134/S1070428006090119
- Dimitrios Kourkoutas, J. Stephen Elmore, Donald S. Mottram. Comparison of the volatile compositions and flavour properties of cantaloupe, Galia and honeydew muskmelons. Food Chemistry 2006, 97
(1)
, 95-102. https://doi.org/10.1016/j.foodchem.2005.03.026
- C. E. Denoon, Homer Adkins, James L. Rainey. Acetylacetone. 2003, 6-6. https://doi.org/10.1002/0471264180.os020.02
- Paulo Gomes, Corinne Gosmini, Jacques Périchon. Cobalt-catalyzed electrochemical vinylation of aryl halides using vinylic acetates. Tetrahedron 2003, 59
(17)
, 2999-3002. https://doi.org/10.1016/S0040-4020(03)00404-6
- Darko Dolenc. Iodination of Enol Acetates and 1,3-Diones Using
N
-Iodosaccharin. Synthetic Communications 2003, 33
(16)
, 2917-2924. https://doi.org/10.1081/SCC-120022182
- Michael A. Walters, Melissa D. Lee. Isopropenyl Acetate. 2001https://doi.org/10.1002/047084289X.ri077
- Claudio Abaecherli, Raimund J. Miller. Ketenes, Ketene Dimers, and Related Substances. 2000https://doi.org/10.1002/0471238961.1105200501020105.a01
- Akihiro Orita, Katsumasa Sakamoto, Yuji Hamada, Akihiro Mitsutome, Junzo Otera. Mild and practical acylation of alcohols with esters or acetic anhydride under distannoxane catalysis. Tetrahedron 1999, 55
(10)
, 2899-2910. https://doi.org/10.1016/S0040-4020(99)00072-1
- Kiyoshi Kudo, Yuji Oida, Koichi Mitsuhashi, Sadayuki Mori, Koichi Komatsu, Nobuyuki Sugita. Hydrocarbonylation of Enol Esters Catalyzed by a Palladium(II) Complex. Bulletin of the Chemical Society of Japan 1996, 69
(5)
, 1337-1345. https://doi.org/10.1246/bcsj.69.1337
- Dominique Limat, Manfred Schlosser. The selective O-acylation of enolates providing a simple entry to O-enesters. Tetrahedron 1995, 51
(20)
, 5799-5806. https://doi.org/10.1016/0040-4020(95)00250-C
- Francisco Fariña, M.Teresa Molina, Pedro Noheda, M.Carmen Paredes. Polycyclic hydroxyquinones. XXVII. Tautomerism in 1,4-Dihydroxy-9,10-anthraquinone Monoimines. Cycloaddition Reactions of Their 1,4-Anthraquinonoid Tautomers. Tetrahedron 1992, 48
(39)
, 8437-8450. https://doi.org/10.1016/S0040-4020(01)86592-3
- Stanley R. Sandler, Wolf Karo. AMIDES. 1992, 92-105. https://doi.org/10.1016/B978-0-08-092553-0.50015-7
- . The synthesis of carboxylic acids and esters and their derivatives. 1991, 1-224. https://doi.org/10.1002/9780470772423.ch1
- Kaspar F. Burri. Tilcotil
® Studies. Part 2. [4 + 2] Additions with Isothiazol‐3(2
H
)‐one 1,1‐Dioxide. Helvetica Chimica Acta 1990, 73
(1)
, 69-80. https://doi.org/10.1002/hlca.19900730107
- Paul F. De Cusati, R.A. Olofson. A simple synthesis of 1-(1,3-butadienyl) carbonates and carbamates. Tetrahedron Letters 1990, 31
(10)
, 1405-1408. https://doi.org/10.1016/S0040-4039(00)88817-6
- Michael J. Taschner, Patrick T. Cyr. Synthesis of tricyclo[6.2.2.01,6]Dodeca-6,9-dienes. An approach to clerodane diterpenes.. Tetrahedron Letters 1990, 31
(37)
, 5297-5300. https://doi.org/10.1016/S0040-4039(00)98054-7
- Boris \u{S}ket, Pavel Zupet, Marko Zupan, Darko Dolenc. α-Iodination of Ketones and Enol Acetates with Poly[styrene-
co
-(4-vinylpyridinium dichloroiodate(1–))]. Bulletin of the Chemical Society of Japan 1989, 62
(10)
, 3406-3408. https://doi.org/10.1246/bcsj.62.3406
- Michael J. Taschner. Synthesis of Clerodane Diterpenes via Lewis Acid Catalyzed Cycloadditions. 1989, 227-246. https://doi.org/10.1007/978-94-009-2464-2_12
- Stojan Stavber, Boris Šket, Barbara Zajc, Marko Zupan. Chemistry of organo halogenic molecules. Part 100. Comparative behaviour of xenon diflouride and caesium fluoroxysulphate in the fluorination of enol acetates and ketones. Tetrahedron 1989, 45
(18)
, 6003-6010. https://doi.org/10.1016/S0040-4020(01)89127-4
- Martin Eberle, Richard G. Lawton. Thioalkylation of
Meldrum
's Acid: Protected alkylidene derivatives of isopropylidene malonate. Helvetica Chimica Acta 1988, 71
(8)
, 1974-1982. https://doi.org/10.1002/hlca.19880710816
- Rolf H. Fischer, Heinz Krapf, Joachim Paust. C5-Bausteine für Terpensynthesen: γ-Acetoxylierung von (E)-2-Methyl-2-butenalen. Angewandte Chemie 1988, 100
(2)
, 301-302. https://doi.org/10.1002/ange.19881000230
- Rolf H. Fischer, Heinz Krapf, Joachim Paust. C
5
Building Blocks for Terpene Syntheses: γ‐Acetoxylation of (
E
)‐2‐Methyl‐2‐butenals. Angewandte Chemie International Edition in English 1988, 27
(2)
, 285-287. https://doi.org/10.1002/anie.198802851
- Jean Barry, Georges Bram, Alain Petit. Organic syntheses without solvent: Base-catalysed ester interchange. Tetrahedron Letters 1988, 29
(36)
, 4567-4568. https://doi.org/10.1016/S0040-4039(00)80548-1
- Wakichi Fukuda, Hozumi Sato, Hiroshi Kakiuchi. Stereoselectivity in the Synthesis of Enol Esters from Chloromercurio Aldehydes and Acyl Chlorides. Bulletin of the Chemical Society of Japan 1986, 59
(3)
, 751-756. https://doi.org/10.1246/bcsj.59.751
- Paul S. Waterman, John E. Belmonte, Thomas E. Bauch, Patricia A. Belmonte, Warren P. Giering. Alkenyliron complexes. Cycloaddition reactions of organoiron metalloalkadienes. Journal of Organometallic Chemistry 1985, 294
(2)
, 235-250. https://doi.org/10.1016/0022-328X(85)87473-8
- A. Tenaglia, P. Brun, B. Waegell. Nickel-catalyzed oligomerization of functionalized conjugated dienes. Journal of Organometallic Chemistry 1985, 285
(1-3)
, 343-357. https://doi.org/10.1016/0022-328X(85)87379-4
- Stanley R. Sandler, Wolf Karo. ESTERS. 1983, 288-314. https://doi.org/10.1016/B978-0-08-092556-1.50014-2
- Stanley R. Sandler, Wolf Karo. AMIDES. 1983, 315-358. https://doi.org/10.1016/B978-0-08-092556-1.50015-4
- Michael E. Garst, Victoria A. Roberts, Calman Prussin. Steric and electronic effects of 1-substituted dienes in cycloaddition reactions with cycloheptatrienone. Tetrahedron 1983, 39
(4)
, 581-589. https://doi.org/10.1016/S0040-4020(01)91832-0
- P. Brun, A. Tenaglia, B. Waegell. Regio and stereo selective synthesis of disubstituted cyclooctadienes.. Tetrahedron Letters 1983, 24
(4)
, 385-388. https://doi.org/10.1016/S0040-4039(00)81414-8
- Ibrahim El‐Sayed El‐Kholy, Morcos Michael Mishrikey, Salah Loutfi Abdoul‐Ela. Preparation and reactions of 3,4‐dihydro‐2
H
‐pyran‐2‐ones. Journal of Heterocyclic Chemistry 1982, 19
(6)
, 1329-1334. https://doi.org/10.1002/jhet.5570190615
- D. Favara, A. Omodei-Salè, P. Consonni, A. Depaoli. A facile synthesis of trans (+)-4-carboxymethyl-3-ethylazetidin-2-one and its conversion into natural PS-5. Tetrahedron Letters 1982, 23
(30)
, 3105-3108. https://doi.org/10.1016/S0040-4039(00)87545-0
- D. M. Nasyrov, A. N. Vereshchagin. Polarity and polarizability of the amide group. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 1981, 30
(3)
, 414-417. https://doi.org/10.1007/BF00949585
- Joaquin Tamariz, Pierre Vogel. New Dienophiles: 1‐Acetylvinyl Arenecarboxylates. Reactivity toward cyclopentadiene and exocyclic dienes. Helvetica Chimica Acta 1981, 64
(1)
, 188-197. https://doi.org/10.1002/hlca.19810640121
- A. Ichihara, M. Ubukata, S. Sakamura. Stereoselective synthesis of (±)-palitantin. Tetrahedron 1980, 36
(11)
, 1547-1550. https://doi.org/10.1016/S0040-4020(01)83120-3
- Karsten Krohn, Klaus Tolkiehn. Synthetische Anthracyclinone, VIII
1)
Totalsynthese des Daunomycinons. Chemische Berichte 1979, 112
(10)
, 3453-3471. https://doi.org/10.1002/cber.19791121013
- Karsten Krohn, Hans‐Hermann Ostermeyer, Klaus Tolkiehn. Synthetische Anthracyclinone, VII. Synthese von DL‐4‐Desmethoxy‐7,10‐ethanodaunomycinon. Chemische Berichte 1979, 112
(7)
, 2640-2649. https://doi.org/10.1002/cber.19791120732
- Y. Tamura, J. Haruta, S. Okuyama, Y. Kita. Preparation and reactions of alkyl and aryl isopropenyl carbonatesnovel alkoxy- and aryloxycarbonylations of amines. Tetrahedron Letters 1978, 19
(39)
, 3737-3740. https://doi.org/10.1016/S0040-4039(01)95045-2
- Akitami Ichihara, Makoto Ubukata, Sadao Sakamura. Stereoselective synthesis of (±)-palitantin. Tetrahedron Letters 1977, 18
(39)
, 3473-3476. https://doi.org/10.1016/S0040-4039(01)83269-X
- Jean‐Claude Gressier, Christian P. Pinazzi, Guy Levesque. Polymérisation et copolymérisation de l'acétoxy‐1 butadiène. Die Makromolekulare Chemie 1975, 176
(2)
, 341-350. https://doi.org/10.1002/macp.1975.021760208
- J. W. Barton. Protection of N—H Bonds and NR3. 1973, 43-93. https://doi.org/10.1007/978-1-4684-7218-9_2
- H. J. E. Loewenthal. Protection of Aldehydes and Ketones. 1973, 323-402. https://doi.org/10.1007/978-1-4684-7218-9_9
- Günter Schmitt, Siegfried Warwel, Eduard Homminga, Wilhelm Meltzow. Reaktionen von Aluminiumalkylen mit Carbonylverbindungen, III
1)
Hydroaluminierung von Ketoenolacetaten, eine neue Synthese von 2.4‐Diolen. Justus Liebigs Annalen der Chemie 1972, 763
(1)
, 75-82. https://doi.org/10.1002/jlac.19727630109
- Victor J Bartuska, Gary E Maciel. Studies of 13C13C coupling constants. IV. The isopropenyl system. Journal of Magnetic Resonance (1969) 1972, 7
(1)
, 36-47. https://doi.org/10.1016/0022-2364(72)90142-4
- A.I. Scott, D.G. Pike, J.J. Ryan, H. Guilford. Biogenetic-type synthesis of polyketides. Part X. Tetrahedron 1971, 27
(14)
, 3051-3063. https://doi.org/10.1016/S0040-4020(01)98098-6
- H. M. R. Hoffmann. The Ene Reaction. Angewandte Chemie International Edition in English 1969, 8
(8)
, 556-577. https://doi.org/10.1002/anie.196905561
- H. M. R. Hoffmann. Die En‐Reaktion. Angewandte Chemie 1969, 81
(16)
, 597-618. https://doi.org/10.1002/ange.19690811603
- John K.G. Kramer, Helmut K. Mangold. Synthesis of 2-alk-1′-enyloxy-ethanols. Chemistry and Physics of Lipids 1969, 3
(2)
, 176-184. https://doi.org/10.1016/0009-3084(69)90009-7
- D. P. N. Satchell, R. S. Satchell. Substitution in the groups COOH and COOR. 1969, 375-452. https://doi.org/10.1002/9780470771099.ch9
- A. Suzuki, K. Ohmori, M. Itoh. The hydroboration of enol acetates derived from aliphatic ketones the directive effect of the acetoxy group. Tetrahedron 1969, 25
(17)
, 3707-3716. https://doi.org/10.1016/S0040-4020(01)82904-5
- G.L. Buchanan, A.C.W. Curran, R.T. Wall. The thermal michael reaction—II. Tetrahedron 1969, 25
(22)
, 5503-5508. https://doi.org/10.1016/S0040-4020(01)83052-0
- Brian C. Challis, Anthony R. Butler. Substitution at an amino nitrogen. 1968, 277-347. https://doi.org/10.1002/9780470771082.ch6
- Eric W. Stern. Reactions of Unsaturated Ligands in Pd(II) Complexes. Catalysis Reviews 1968, 1
(1)
, 73-152. https://doi.org/10.1080/01614946808064701
- V. A. Vaver, V. V. Dorogov, L. D. Bergel'son. Dipole lipids. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 1967, 16
(12)
, 2555-2557. https://doi.org/10.1007/BF00908495
- Hans Schick, Gerhard Lehmann, Günter Hilgetag. Synthese von 2‐Alkyl‐1,3‐diketonen durch Bisacylierung von Enolacetaten. Journal für Praktische Chemie 1967, 35
(1-2)
, 28-35. https://doi.org/10.1002/prac.19670350105
- E.W. Stern, M.L. Spector, H.P. Leftin. The reaction of vinyl halide-palladium(II) chloride complexes with nucleophiles: Catalytic vinylation. Journal of Catalysis 1966, 6
(1)
, 152-153. https://doi.org/10.1016/0021-9517(66)90121-7
- Roy C. De Selms. A new method of ring expansion. Tetrahedron Letters 1966, 7
(18)
, 1965-1968. https://doi.org/10.1016/S0040-4039(00)76279-4
- Hermann G. Hauthal, Peter Kluge, Harald Schmidt. Zur Herstellung sterisch gehinderter Enolacetate. Journal für Praktische Chemie 1965, 29
(3-4)
, 296-299. https://doi.org/10.1002/prac.19650290317
- Norman S. Radin. The hydroxy fatty acids: Isolation, structure determination, quantitation. Journal of the American Oil Chemists' Society 1965, 42
(7)
, 569-580. https://doi.org/10.1007/BF02541292
- Masamichi Kusunose, Emi Kusunose, Minor J. Coon. Enzymatic ω-Oxidation of Fatty Acids. Journal of Biological Chemistry 1964, 239
(5)
, 1374-1380. https://doi.org/10.1016/S0021-9258(18)91324-4
- Hans Muxfeldt, Goetz Hardtmann. Tetracycline, V. Modellversuche zum Aufbau des Terramycins. Justus Liebigs Annalen der Chemie 1963, 669
(1)
, 113-120. https://doi.org/10.1002/jlac.19636690113
- Amiya K. Hajra, Norman S. Radin. Isotopic studies of the biosynthesis of the cerebroside fatty acids in rats. Journal of Lipid Research 1963, 4
(3)
, 270-278. https://doi.org/10.1016/S0022-2275(20)40301-3
- Yasuo Kishimoto, Norman S. Radin. Microdetermination, isolation, and gas-liquid chromatography of 2-hydroxy fatty acids. Journal of Lipid Research 1963, 4
(2)
, 130-138. https://doi.org/10.1016/S0022-2275(20)40338-4
- G. QUADBECK. Ketene in Preparative Organic Chemistry. 1963, 133-161. https://doi.org/10.1016/B978-0-12-395648-4.50012-X
- R. Filler, S.M. Naqvi. Fluorine-containing β-dicarbonyl compounds. Tetrahedron 1963, 19
(6)
, 879-889. https://doi.org/10.1016/S0040-4020(01)99342-1
- Ulrich Schmidt, Paul Grafen. Ozonisierung cyclischer Enoläther. ω‐Aldehydsäuren und ω‐Hydroxyaldehyde aus cyclischen Ketonen. Justus Liebigs Annalen der Chemie 1962, 656
(1)
, 97-102. https://doi.org/10.1002/jlac.19626560115
- F. Weygand, W. Steglich. Peptid‐Synthesen mit Acylaminosäure‐vinylestern. Angewandte Chemie 1961, 73
(23)
, 757-757. https://doi.org/10.1002/ange.19610732308
- Pierre‐Yves Blanc. Etude de quelques énolacylates diéniques et leur utilisation dans une méthode générale de synthèse d'anhydrides phtaliques substitués. Helvetica Chimica Acta 1961, 44
(1)
, 1-12. https://doi.org/10.1002/hlca.19610440102
- A.V. TOPCHIEV, S.V. ZAVGORODNII, Ya.M. PAUSHKIN. THE ADDITION OF ORGANIC SUBSTANCES CONTAINING OXYGEN OR SULPHUR TO ETHYLENIC COMPOUNDS. 1958, 205-226. https://doi.org/10.1016/B978-0-08-009128-0.50011-2
Article Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.
Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.
The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated.