Synthetic Studies on the Bryostatins: Preparation of a Truncated BC-Ring Intermediate by Pyran Annulation
- 28 April 2005
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 7 (11) , 2149-2152
- https://doi.org/10.1021/ol050511w
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Enantio- and Diastereoselective Additions to Aldehydes Using the Bifunctional Reagent 2-(Chloromethyl)-3-(tributylstannyl)propene: Application to a Synthesis of the C16−C27 Segment of Bryostatin 1The Journal of Organic Chemistry, 2005
- Concise Formal Synthesis of the Bryostatin Southern Hemisphere (C17−C27)The Journal of Organic Chemistry, 2004
- Total Synthesis of Bryostatin 2Journal of the American Chemical Society, 1999
- Synthesis of the First Members of a New Class of Biologically Active Bryostatin AnaloguesJournal of the American Chemical Society, 1998
- A Stereochemical Model for Merged 1,2- and 1,3-Asymmetric Induction in Diastereoselective Mukaiyama Aldol Addition Reactions and Related ProcessesJournal of the American Chemical Society, 1996
- Diastereoselective Aldol and Allylstannane Addition Reactions. The Merged Stereochemical Impact of .alpha. and .beta. Aldehyde SubstituentsJournal of the American Chemical Society, 1995
- Practical, high-yield, regioselective, rhodium-catalyzed hydroformylation of functionalized .alpha.-olefinsJournal of the American Chemical Society, 1993
- Synthesis of bryostatin 7Journal of the American Chemical Society, 1990
- Dramatic effects of oxygen substituents on 1,3-asymmetric induction in additions of allyltriphenylstannane to .beta.-alkoxy aldehydes: a chemical and spectroscopic investigationThe Journal of Organic Chemistry, 1986
- Isolation and structure of bryostatin 1Journal of the American Chemical Society, 1982