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Total Synthesis of Longifolene

Cite this: J. Am. Chem. Soc. 1964, 86, 3, 478–485
Publication Date (Print):February 1, 1964
https://doi.org/10.1021/ja01057a039
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    10. Terry P. Lebold, Gary M. Gallego, Christopher J. Marth, and Richmond Sarpong . Synthesis of the Bridging Framework of Phragmalin-Type Limonoids. Organic Letters 2012, 14 (8) , 2110-2113. https://doi.org/10.1021/ol300647k
    11. Zhen-Lei Song, Chun-An Fan, and Yong-Qiang Tu . Semipinacol Rearrangement in Natural Product Synthesis. Chemical Reviews 2011, 111 (11) , 7523-7556. https://doi.org/10.1021/cr200055g
    12. David C. Moebius and Jason S. Kingsbury. Catalytic Homologation of Cycloalkanones with Substituted Diazomethanes. Mild and Efficient Single-Step Access to α-Tertiary and α-Quaternary Carbonyl Compounds. Journal of the American Chemical Society 2009, 131 (3) , 878-879. https://doi.org/10.1021/ja809220j
    13. Kelly A. Fairweather and, Lewis N. Mander. A Formal Total Synthesis of the Marine Diterpenoid Diisocyanoadociane. Organic Letters 2006, 8 (15) , 3395-3398. https://doi.org/10.1021/ol061228f
    14. Beth E. Jackson,, Elizabeth A. Hart-Wells, and, Seiichi P. T. Matsuda. Metabolic Engineering to Produce Sesquiterpenes in Yeast. Organic Letters 2003, 5 (10) , 1629-1632. https://doi.org/10.1021/ol034231x
    15. Gilbert Stork,, Fred West,, Hee Yoon Lee,, Richard C. A. Isaacs, and, Shino Manabe. The Total Synthesis of a Natural Cardenolide:  (+)-Digitoxigenin. Journal of the American Chemical Society 1996, 118 (43) , 10660-10661. https://doi.org/10.1021/ja962163m
    16. Goh Sennari, Richmond Sarpong. Use of Emerging C-H Functionalization Methods to Implement Strategies for the Divergent Total Syntheses of Bridged Polycyclic Natural Products. Journal of Synthetic Organic Chemistry, Japan 2023, 81 (11) , 1028-1039. https://doi.org/10.5059/yukigoseikyokaishi.81.1028
    17. Bo Yin, Xiaohuan Li, Zi‐Xiang Li, Xiao‐Xin Zhu, Lan Zhang, Xian‐Li Zhou, Jin‐Bu Xu, Feng‐Zheng Chen, Pei Tang, Feng Gao. Adenophorone, An Unprecedented Sesquiterpene from Eupatorium adenophorum : Structural Elucidation, Bioinspired Total Synthesis and Neuroprotective Activity Evaluation. Angewandte Chemie 2023, 135 (31) https://doi.org/10.1002/ange.202306326
    18. Bo Yin, Xiaohuan Li, Zi‐Xiang Li, Xiao‐Xin Zhu, Lan Zhang, Xian‐Li Zhou, Jin‐Bu Xu, Feng‐Zheng Chen, Pei Tang, Feng Gao. Adenophorone, An Unprecedented Sesquiterpene from Eupatorium adenophorum : Structural Elucidation, Bioinspired Total Synthesis and Neuroprotective Activity Evaluation. Angewandte Chemie International Edition 2023, 62 (31) https://doi.org/10.1002/anie.202306326
    19. Haoyu Wang, Guanghao Wei, , . Introduction to Retrosynthesis: Strategies and Approaches. E3S Web of Conferences 2023, 385 , 04008. https://doi.org/10.1051/e3sconf/202338504008
    20. Robert F. Lusi, Goh Sennari, Richmond Sarpong. Total synthesis of nine longiborneol sesquiterpenoids using a functionalized camphor strategy. Nature Chemistry 2022, 14 (4) , 450-456. https://doi.org/10.1038/s41557-021-00870-4
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    23. Yujin Cao, Rubing Zhang, Wei Liu, Guang Zhao, Wei Niu, Jiantao Guo, Mo Xian, Huizhou Liu. Manipulation of the precursor supply for high-level production of longifolene by metabolically engineered Escherichia coli. Scientific Reports 2019, 9 (1) https://doi.org/10.1038/s41598-018-36495-w
    24. Carles Rodríguez‐Escrich, Miquel A. Pericàs. Catalytic Enantioselective Flow Processes with Solid‐Supported Chiral Catalysts. The Chemical Record 2019, 19 (9) , 1872-1890. https://doi.org/10.1002/tcr.201800097
    25. Jeffrey I. Seeman. On the Relationship between Classical Structure Determination and Retrosynthetic Analysis/Total Synthesis †. Israel Journal of Chemistry 2018, 58 (1-2) , 28-44. https://doi.org/10.1002/ijch.201700079
    26. Lidia Clot-Almenara, Carles Rodríguez-Escrich, Miquel A. Pericàs. Desymmetrisation of meso -diones promoted by a highly recyclable polymer-supported chiral phosphoric acid catalyst. RSC Advances 2018, 8 (13) , 6910-6914. https://doi.org/10.1039/C7RA13471A
    27. Guangkuan Zhao, Ling‐Zhi Yuan, Mouad Alami, Olivier Provot. Desulfurization of Thioketals into Methylene and Methyl Derivatives: Nickel or not Nickel?. ChemistrySelect 2017, 2 (33) , 10951-10959. https://doi.org/10.1002/slct.201702370
    28. Nikolaos Drosos, Gui‐Juan Cheng, Erhan Ozkal, Bastien Cacherat, Walter Thiel, Bill Morandi. Catalytic Reductive Pinacol‐Type Rearrangement of Unactivated 1,2‐Diols through a Concerted, Stereoinvertive Mechanism. Angewandte Chemie 2017, 129 (43) , 13562-13566. https://doi.org/10.1002/ange.201704936
    29. Nikolaos Drosos, Gui‐Juan Cheng, Erhan Ozkal, Bastien Cacherat, Walter Thiel, Bill Morandi. Catalytic Reductive Pinacol‐Type Rearrangement of Unactivated 1,2‐Diols through a Concerted, Stereoinvertive Mechanism. Angewandte Chemie International Edition 2017, 56 (43) , 13377-13381. https://doi.org/10.1002/anie.201704936
    30. Jeffrey I. Seeman. Synthesis and the Nobel Prize in Chemistry. Nature Chemistry 2017, 9 (10) , 925-929. https://doi.org/10.1038/nchem.2864
    31. Richard C. Larock, Xiaoxia Zhang. Formation of Alkanes and Arenes by Reduction. 2017, 1-189. https://doi.org/10.1002/9781118662083.cot01-001
    32. John Andraos. A new paradigm for designing ring construction strategies for green organic synthesis: implications for the discovery of multicomponent reactions to build molecules containing a single ring. Beilstein Journal of Organic Chemistry 2016, 12 , 2420-2442. https://doi.org/10.3762/bjoc.12.236
    33. Sunil Kumar Talapatra, Bani Talapatra. Sesquiterpenoids (C15). 2015, 403-468. https://doi.org/10.1007/978-3-642-45410-3_7
    34. Keiji Mori, Ayaka Miyake, Takahiko Akiyama. Enantioselective synthesis of fused heterocycles with contiguous stereogenic centers by chiral phosphoric acid catalyzed symmetry breaking. Chemical Communications 2015, 51 (89) , 16107-16110. https://doi.org/10.1039/C5CC05508C
    35. Leandro de C. Alves, André L. Desiderá, Kleber T. de Oliveira, Sean Newton, Steven V. Ley, Timothy J. Brocksom. A practical deca-gram scale ring expansion of (R)-(−)-carvone to (R)-(+)-3-methyl-6-isopropenyl-cyclohept-3-enone-1. Organic & Biomolecular Chemistry 2015, 13 (28) , 7633-7642. https://doi.org/10.1039/C5OB00525F
    36. Kleber T. de Oliveira, Bruno M. Servilha, Leandro de C. Alves, André L. Desiderá, Timothy J. Brocksom. The Synthesis of Seven-Membered Rings in Natural Products. 2014, 421-463. https://doi.org/10.1016/B978-0-444-63281-4.00014-8
    37. Wei Li, Xiaohua Liu, Fei Tan, Xiaoyu Hao, Jianfeng Zheng, Lili Lin, Xiaoming Feng. Catalytic Asymmetric Homologation of α‐Ketoesters with α‐Diazoesters: Synthesis of Succinate Derivatives with Chiral Quaternary Centers. Angewandte Chemie 2013, 125 (41) , 11083-11086. https://doi.org/10.1002/ange.201305478
    38. Wei Li, Xiaohua Liu, Fei Tan, Xiaoyu Hao, Jianfeng Zheng, Lili Lin, Xiaoming Feng. Catalytic Asymmetric Homologation of α‐Ketoesters with α‐Diazoesters: Synthesis of Succinate Derivatives with Chiral Quaternary Centers. Angewandte Chemie International Edition 2013, 52 (41) , 10883-10886. https://doi.org/10.1002/anie.201305478
    39. Reinhard W. Hoffmann. Naturstoffsynthese im Wandel der Zeit. Angewandte Chemie 2013, 125 (1) , 133-140. https://doi.org/10.1002/ange.201203319
    40. Reinhard W. Hoffmann. Natural Product Synthesis: Changes over Time. Angewandte Chemie International Edition 2013, 52 (1) , 123-130. https://doi.org/10.1002/anie.201203319
    41. Jonathan William Medley, Mohammad Movassaghi. Robinson's landmark synthesis of tropinone. Chemical Communications 2013, 49 (92) , 10775. https://doi.org/10.1039/c3cc44461a
    42. Lin Yang, Li-Rui Qiao, Jian-Jun Zhang, Jun-Gui Dai, Shun-Xing Guo. Two new sesquiterpene derivatives from Chinese eaglewood. Journal of Asian Natural Products Research 2012, 14 (11) , 1054-1058. https://doi.org/10.1080/10286020.2012.704910
    43. Jitender M. Khurana, Devanshi Magoo. Nickel Boride–Mediated Cleavage of 1,3-Dithiolanes: A Convenient Approach to Reductive Desulfurization. Synthetic Communications 2010, 40 (19) , 2908-2913. https://doi.org/10.1080/00397910903340652
    44. Keiji Mori, Takuya Katoh, Tohru Suzuki, Takuya Noji, Masahiro Yamanaka, Takahiko Akiyama. Chiral Phosphoric Acid Catalyzed Desymmetrization of meso ‐1,3‐Diones: Asymmetric Synthesis of Chiral Cyclohexenones. Angewandte Chemie 2009, 121 (51) , 9832-9834. https://doi.org/10.1002/ange.200905271
    45. Keiji Mori, Takuya Katoh, Tohru Suzuki, Takuya Noji, Masahiro Yamanaka, Takahiko Akiyama. Chiral Phosphoric Acid Catalyzed Desymmetrization of meso ‐1,3‐Diones: Asymmetric Synthesis of Chiral Cyclohexenones. Angewandte Chemie International Edition 2009, 48 (51) , 9652-9654. https://doi.org/10.1002/anie.200905271
    46. William Goodwin. Scientific Understanding and Synthetic Design. The British Journal for the Philosophy of Science 2009, 60 (2) , 271-301. https://doi.org/10.1093/bjps/axp010
    47. Gopal Subramaniam, Varsha Patel, Sasan Karimi. Conformational Analysis of Longifolene. Spectroscopy Letters 2008, 41 (7) , 349-353. https://doi.org/10.1080/00387010802371528
    48. W. M. Goodwin. Implementation and innovation in total synthesis. Foundations of Chemistry 2008, 10 (3) , 177-186. https://doi.org/10.1007/s10698-008-9050-9
    49. Kelly A. Fairweather, Simon R. Crabtree, Lewis N. Mander. Chapter 2 A formal total synthesis of the marine diterpenoid, diisocyanoadociane. 2008, 35-58. https://doi.org/10.1016/S1874-6004(08)80006-8
    50. Thomas J Maimone, Phil S Baran. Modern synthetic efforts toward biologically active terpenes. Nature Chemical Biology 2007, 3 (7) , 396-407. https://doi.org/10.1038/nchembio.2007.1
    51. Gerhard Quinkert, Holger Wallmeier, Norbert Windhab, Dietmar Reichert. Chemistry and Biology — Historical and Philosophical Aspects. 2007, 3-67. https://doi.org/10.1002/9783527619375.ch1
    52. Gopal Subramaniam, Sasan Karimi, David Phillips. Solution conformation of longifolene and its precursor by NMR and ab initio calculations. Magnetic Resonance in Chemistry 2006, 44 (12) , 1118-1121. https://doi.org/10.1002/mrc.1908
    53. Prasad Appukkuttan, Erik Van der Eycken. Microwave-Assisted Natural Product Chemistry. 2006, 1-47. https://doi.org/10.1007/128_051
    54. Thomas P. Brady, Sun Hee Kim, Ke Wen, Charles Kim, Emmanuel A. Theodorakis. Norrisolide: Total Synthesis and Related Studies. Chemistry – A European Journal 2005, 11 (24) , 7175-7190. https://doi.org/10.1002/chem.200500513
    55. Thomas P. Brady, Sun Hee Kim, Ke Wen, Emmanuel A. Theodorakis. Stereoselective Total Synthesis of (+)‐Norrisolide. Angewandte Chemie 2004, 116 (6) , 757-760. https://doi.org/10.1002/ange.200352868
    56. Thomas P. Brady, Sun Hee Kim, Ke Wen, Emmanuel A. Theodorakis. Stereoselective Total Synthesis of (+)‐Norrisolide. Angewandte Chemie International Edition 2004, 43 (6) , 739-742. https://doi.org/10.1002/anie.200352868
    57. Ludmila Birladeanu. Die Geschichte von Santonin und Santonsäure. Angewandte Chemie 2003, 115 (11) , 1236-1242. https://doi.org/10.1002/ange.200390289
    58. Ludmila Birladeanu. The Stories of Santonin and Santonic Acid. Angewandte Chemie International Edition 2003, 42 (11) , 1202-1208. https://doi.org/10.1002/anie.200390318
    59. Vladimir Dimitrov, Gudrun Hopp Rentsch, Anthony Linden, Manfred Hesse. The Ozonolysis of Longifolene: A Tool for the Preparation of Useful Chiral Compounds. Configuration Determination of New Stereogenic Centers by NMR Spectroscopy and X‐Ray Crystallography. Helvetica Chimica Acta 2003, 86 (1) , 106-121. https://doi.org/10.1002/hlca.200390000
    60. R. Barone, M. Petitjean, C. Baralotto, P. Piras, M. Chanon. Information theory description of synthetic strategies. A new similarity index. Journal of Physical Organic Chemistry 2003, 16 (1) , 9-15. https://doi.org/10.1002/poc.556
    61. D Rajagopal, R Narayanan, S Swaminathan. Enantioselective solvent-free Robinson annulation reactions. Journal of Chemical Sciences 2001, 113 (3) , 197-213. https://doi.org/10.1007/BF02704070
    62. William Reusch. Calcium Carbonate. 2001https://doi.org/10.1002/047084289X.rc004
    63. Raymond E. Conrow. 1,2-Ethanedithiol. 2001https://doi.org/10.1002/047084289X.re008
    64. Francis A. Carey, Richard J. Sundberg. Planning and Execution of Multistep Syntheses. 2001, 821-922. https://doi.org/10.1007/978-3-662-39510-3_13
    65. Timothy John Brocksom, Arlene G. Corrêa, Ronilda M. Naves, Fausto Silva, Valdomiro Catani, Marco A. Ceschi, Julio Zukerman-Schpector, Ana Paula Toloi, Maria Lúcia Ferreira, Ursula Brocksom. Diels-Alder reactions in the synthesis of higher terpenes. 2001, 39-87. https://doi.org/10.1016/S1047-773X(01)80003-2
    66. Gérard Taurand. Phenothiazine and Derivatives. 2000https://doi.org/10.1002/14356007.a19_387
    67. Eric J. Kantorowski, Mark J. Kurth. Expansion to Seven-Membered Rings. Tetrahedron 2000, 56 (26) , 4317-4353. https://doi.org/10.1016/S0040-4020(00)00218-0
    68. A.K. Banerjee, M. Laya-Mimo. Synthesis of Bioactive Terpenes from Wieland-Miescher Ketone and its Methyl Analog† †To the memory of Professor D. H. R. Barton whose work and worth will not be forgotten.. 2000, 175-213. https://doi.org/10.1016/S1572-5995(00)80046-0
    69. Robert E. Gawley. Stereoselective addition of chiral α-aminoorganometallics to aldehydes. 1999, 77-111. https://doi.org/10.1016/S1874-5148(98)80005-5
    70. B.N. Naidu, F.G. West. A short, enantioselective synthesis of (−)-epilupinine from proline via a spirocyclic ammonium ylide. Tetrahedron 1997, 53 (48) , 16565-16574. https://doi.org/10.1016/S0040-4020(97)01037-5
    71. Tse‐Lok Ho, Yueh‐Jyh Lin. Synthesis and Properties of 3‐Thia‐9‐azabicyclo[3.3.1]nonan‐7‐one. Journal of the Chinese Chemical Society 1997, 44 (3) , 261-263. https://doi.org/10.1002/jccs.199700040
    72. Paola Ciceri, F.W.Joachim Demnitz. An efficient, rapid and highly selective preparation of the Wieland-Miescher ketone-9-ethylene ketal. Tetrahedron Letters 1997, 38 (3) , 389-390. https://doi.org/10.1016/S0040-4039(96)02334-9
    73. Lynda J. Benjamin, Lewis N. Mander, Anthony C. Willis. Conversion of a gibberellin aldehyde into a 20-norkaurenoid lactone. Tetrahedron Letters 1996, 37 (49) , 8937-8940. https://doi.org/10.1016/S0040-4039(96)02052-7
    74. Yasuyuki Ueki, Masanori Itoh, Tadashi Katoh, Shiro Terashima. Synthesis of various model compounds for the central tricyclic ring system of popolophuanone E. Tetrahedron Letters 1996, 37 (32) , 5719-5722. https://doi.org/10.1016/0040-4039(96)01209-9
    75. . Chapter 7 7. Systems with unusual structural features: Quaternary carbon atoms, medium-sized rings and bridged systems. 1996, 181-213. https://doi.org/10.1016/S0165-3253(96)80013-7
    76. R. Daniel Little, Mohammad R. Masjedizadeh, Olof Wallquist, Jim I. Mcloughlin. The Intramolecular M ichael Reaction. 1995, 315-552. https://doi.org/10.1002/0471264180.or047.02
    77. P. M. Imamura, R. T. Nogueira. A Convenient Synthesis of C-8 Oxo-eudesmane. Total Synthesis of (±)-Eudesma-5,7(11)-dien-8-one. Synthetic Communications 1995, 25 (3) , 405-412. https://doi.org/10.1080/00397919508011372
    78. Iain Coldham. One or More CH and/or CC Bond(s) Formed by Rearrangement. 1995, 377-423. https://doi.org/10.1016/B0-08-044705-8/00151-5
    79. . References to Volume 1. 1995, 1147-1316. https://doi.org/10.1016/B0-08-044705-8/09009-9
    80. H. John, Tyman P.. The Role of Biological Raw Materials in Synthesis. 1995, 601-654. https://doi.org/10.1016/S1572-5995(05)80096-1
    81. Tadafumi Uchimaru, Kazutoshi Tanabe. Organic synthesis design system CASINO. 1994, 567-570. https://doi.org/10.1016/B978-0-444-81993-2.50137-2
    82. Feng Wang, Kazuhiro Chiba, Masahiro Tada. Stereoselective Synthesis of (±)-7β-Acetoxyvouacapane. Chemistry Letters 1993, 22 (12) , 2117-2120. https://doi.org/10.1246/cl.1993.2117
    83. Tadafumi Uchimaru, Kazutoshi Tanabe. Organic synthesis design system CASINO. 1993, 973-978. https://doi.org/10.1016/B978-0-444-89778-7.50028-1
    84. Clayton H. Heathcock. Die faszinierenden Alkaloide aus Yuzuriha. Angewandte Chemie 1992, 104 (6) , 675-691. https://doi.org/10.1002/ange.19921040604
    85. Clayton H. Heathcock. The Enchanting Alkaloids of Yuzuriha. Angewandte Chemie International Edition in English 1992, 31 (6) , 665-681. https://doi.org/10.1002/anie.199206653
    86. . Cycloalkenones. 1992, 137-197. https://doi.org/10.1016/B978-0-08-037067-5.50009-6
    87. Raymond J. Giguere. Microwave-Assisted Organic Synthesis. MRS Proceedings 1992, 269 https://doi.org/10.1557/PROC-269-387
    88. Simeon Arséniyadis, Ricardo Rodriguez, Eduardo Cabrera, Adrian Thompson, Guy Ourisson. Synthetic approaches to pentacyclic triterpenes of the arborane family. Tetrahedron 1991, 47 (34) , 7045-7058. https://doi.org/10.1016/S0040-4020(01)96159-9
    89. Elias James Corey. Die Logik der chemischen Synthese: Vielstufige Synthesen komplexer „carbogener”︁ Moleküle (Nobel‐Vortrag). Angewandte Chemie 1991, 103 (5) , 469-479. https://doi.org/10.1002/ange.19911030504
    90. Elias James Corey. The Logic of Chemical Synthesis: Multistep Synthesis of Complex Carbogenic Molecules (Nobel Lecture). Angewandte Chemie International Edition in English 1991, 30 (5) , 455-465. https://doi.org/10.1002/anie.199104553
    91. Christina L. Leone, A.Richard Chamberlin. Lithium aluminum hydride reduction of N-aziridinylimines to hydrocarbons. Tetrahedron Letters 1991, 32 (14) , 1691-1694. https://doi.org/10.1016/S0040-4039(00)74305-X
    92. J. D. Connolly, R. A. Hill. Sesquiterpenoids. 1991, 153-653. https://doi.org/10.1007/978-1-4899-4513-6_3
    93. Bruce Rickborn. The Pinacol Rearrangement. 1991, 721-732. https://doi.org/10.1016/B978-0-08-052349-1.00078-0
    94. Robert G. Salomon. Synthesis of a Cancer Growth-Inhibiting Diterpene: Spatol. 1991, 381-416. https://doi.org/10.1016/B978-0-08-092430-4.50016-0
    95. Francis A. Carey, Richard J. Sundberg. Alkylation of Nucleophilic Carbon. Enolates and Enamines. 1990, 1-54. https://doi.org/10.1007/978-1-4613-9797-7_1
    96. Francis A. Carey, Richard J. Sundberg. Multistep Syntheses. 1990, 677-761. https://doi.org/10.1007/978-1-4613-9797-7_13
    97. . Systems with Unusual Structural Features: Quaternary Carbon Atoms, Medium-Sized Rings and Bridged Systems. 1990, 160-184. https://doi.org/10.1016/B978-0-444-88345-2.50014-6
    98. David A. Oare, Clayton H. Heathcock. Stereochemistry of the Base‐Promoted Michael Addition Reaction. 1989, 227-407. https://doi.org/10.1002/9780470147283.ch5
    99. Robin A.J. Smith, A.Samuel Vellekoop. An investigation of the electron transfer properties of modified organocofper reagents and higher-order cuprates. Tetrahedron 1989, 45 (2) , 517-522. https://doi.org/10.1016/0040-4020(89)80079-1
    100. Makoto Yanagawa, Osamu Moriya, Yoshihiko Watanabe, Yoshio Ueno, Takeshi Endo. A New Synthetic Route to Aliphatic and Alicyclic Nitriles via Homolytic Desulfurization of α-(Dithiocarbamoylthio) Nitriles. Bulletin of the Chemical Society of Japan 1988, 61 (6) , 2203-2204. https://doi.org/10.1246/bcsj.61.2203
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