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Research Article

Stereochemistry of the Robinson-Schoepf reaction. A stereospecific total synthesis of the ladybug defense alkaloids precoccinelline and coccinelline

Robert V. Stevens, Albert W. M. Lee

J. Am. Chem. Soc., 1979, 101 (23), pp 7032–7035

DOI: 10.1021/ja00517a042

Publication Date: November 1979

Note: In lieu of an abstract, this is the article's first page.

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Enantiospecific Total Syntheses of Kapakahines B and FJournal of the American Chemical Society
- Enantiospecific Total Syntheses of Kapakahines B and F
  Timothy Newhouse, Chad A. Lewis and Phil S. Baran
  Journal of the American Chemical Society 2009 131 (18), pp 6360–6361
  Abstract: Gram-scale, enantiospecific total syntheses of the anti-leukemia marine natural products kapakahines B and F have been completed. Two powerfully simplifying transformations have enabled the gram-scale synthesis of this natural product family: (1) an ...
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Total synthesis of (+-)-porantherineJournal of the American Chemical Society
- Total synthesis of (+-)-porantherine
  E. J. Corey, Richard D. Balanson
  Journal of the American Chemical Society 1974 96 (20), pp 6516–6517
  Abstract | Hi-Res PDF
Total Synthesis of the Akuammiline Alkaloid (±)-VincorineJournal of the American Chemical Society
- Total Synthesis of the Akuammiline Alkaloid (±)-Vincorine
  Min Zhang, Xiaoping Huang, Liqun Shen and Yong Qin
  Journal of the American Chemical Society 2009 131 (16), pp 6013–6020
  Abstract: The first total synthesis of the akuammiline alkaloid (±)-vincorine (6) has been accomplished in about 1% overall yield in 31 steps. A concise assembly of the core 1,2-disubstituted 1,2,3,4-tetrahydro-4a,9a-iminoethanocarbazole (1), a distinctive feature ...
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