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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 34, 2004 - Issue 21
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Original Articles

A Concise Synthesis of (±)‐Sporochnol A

Shaojun Shan Guangzhou Institute of Chemistry, Chinese Academy of Sciences, P.O. Box 1122, Guangzhou, 510650, China
&
Chengyong Ha Guangzhou Institute of Chemistry, Chinese Academy of Sciences, P.O. Box 1122, Guangzhou, 510650, China
Pages 4005-4008 | Received 24 May 2004, Published online: 10 Jan 2011

Citations (8)

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Read on this site (1)

A. Srikrishna, G. Satyanarayana & M. R. Prasad. (2005) Synthetic Approaches to Sporochnols A–C. Synthetic Communications 35:12, pages 1687-1698.
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Articles from other publishers (7)

Muhammad Salman, Yaoyao Xu, Shahid Khan, Junjie Zhang & Ajmal Khan. (2020) Regioselective molybdenum-catalyzed allylic substitution of tertiary allylic electrophiles: methodology development and applications. Chemical Science 11:21, pages 5481-5486.
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Yuichi Kobayashi, Yusuke Sugihara, Toshifumi Tojo & Takuri Ozaki. (2016) Synthesis of (S)- and (R)-Sporochnol by Using the Allylic Substitution of the Secondary Allylic Picolinate. HETEROCYCLES 93:1, pages 47.
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Rubén Martín & Stephen L. Buchwald. (2008) An Improved Protocol for the Pd-Catalyzed α-Arylation of Aldehydes with Aryl Halides. Organic Letters 10:20, pages 4561-4564.
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Constanze Brocke, Marcus Eh & Anja Finke. (2008) Recent Developments in the Chemistry of Sandalwood Odorants. Chemistry & Biodiversity 5:6, pages 1000-1010.
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Ramón Alibés, Félix Busqué, Gisela G. Bardají, Pedro de March, Marta Figueredo & Josep Font. (2006) A short and efficient synthesis of (R)-(−)-sporochnol A. Tetrahedron: Asymmetry 17:18, pages 2632-2636.
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Masao Morita, Satoshi Sakaguchi & Yasutaka Ishii. (2006) One-Pot Synthesis of γ,δ-Unsaturated Carbonyl Compounds from Allyl Alcohols and Vinyl or Isopropenyl Acetates Catalyzed by [IrCl(cod)] 2 . The Journal of Organic Chemistry 71:16, pages 6285-6286.
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Shaojun Shan & Chengyong Ha. (2005) A Concise Synthesis of (.+‐.)‐Sporochnol A. ChemInform 36:10.
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