Efficient Asymmetric Synthesis of the C9−C21 Portion of the Aplysiatoxin and Oscillatoxin Marine Natural Products
- 1 November 1998
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 63 (24) , 9113-9116
- https://doi.org/10.1021/jo981370x
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Improved Procedure for the Reduction of N-AcyloxazolidinonesSynthetic Communications, 1990
- Synthetic study on aplysiatoxins, highly inflammatory agents and tumor promoters synthesis of the three optically active segmentsTetrahedron Letters, 1989
- An approach to the total synthesis of aplysiatoxinJournal of the American Chemical Society, 1988
- A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep synthesesJournal of the American Chemical Society, 1987
- Total synthesis of debromoaplysiatoxin and aplysiatoxinJournal of the American Chemical Society, 1987
- Structures and stereochemistries of oscillatoxin B, 31-noroscillatoxin B, oscillatoxin D, and 30-methyloscillatoxin DThe Journal of Organic Chemistry, 1985
- Activation of calcium-activated, phospholipid-dependent protein kinase (protein kinase C) by new classes of tumor promoters: Teleocidin and debromoaplysiatoxinBiochemical and Biophysical Research Communications, 1984
- New classes of environmental tumor promoters: indole alkaloids and polyacetates.Environmental Health Perspectives, 1983
- Alkylation of Ketones and Aldehydes via their Nitrogen DerivativesSynthesis, 1983
- Total synthesis of (+-)-vermiculineJournal of the American Chemical Society, 1975