Synthetic studies on bryostatins, antineoplastic metabolites: Convergent synthesis of the C1-C16 fragment shared by all of the bryostatin family
- 1 July 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (31) , 4981-4984
- https://doi.org/10.1016/s0040-4039(00)74063-9
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Bryostatins revisited: a new bryostatin 3 and the use of NMR to determine stereochemistry in the C-20-C-23 areaThe Journal of Organic Chemistry, 1992
- Revised structure of bryostatin 3 and isolation of the bryostatin 3 26-ketone from Bugula neritinaThe Journal of Organic Chemistry, 1991
- Synthesis of 1,3-diol synthons from epoxy aromatic precursors: an approach to the construction of polyacetate-derived natural productsThe Journal of Organic Chemistry, 1991
- A Chemoenzymatic Synthesis of the C1-C9 Fragment of Bryostatin. Unusual Diastereoselectivity During a Mukaiyama Aldol CondensationSynlett, 1990
- Synthesis of bryostatins. 1. Construction of the C(1)-C(16) fragmentThe Journal of Organic Chemistry, 1989
- Magnesium Bromide Mediated Selective Conversion of Acetals into ThioacetalsChemistry Letters, 1989
- Stereoselective exocyclic double bond formation via vinyl radical cyclizationJournal of the Chemical Society, Chemical Communications, 1989
- Synthesis of 1,3-dioxin-4-ones and their use in synthesis.Journal of Synthetic Organic Chemistry, Japan, 1988
- Asymmetric Photocycloadditions with Optically Pure, Spirocyclic Enones. Simple Synthesis of (+)‐ and (−)‐GrandisolAngewandte Chemie International Edition in English, 1986
- Cram rule selectivity in the Lewis acid catalyzed cyclocondensation of chiral aldehydes. A convenient route to chiral systems of biological interestThe Journal of Organic Chemistry, 1982