Total Synthesis of (−)-Spongidepsin
Author:
Affiliation:
1. ESPCI, Laboratoire de Chimie Organique, 10 Rue Vauquelin, 75231 Paris Cedex 05, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol061029w
Reference11 articles.
1. Spongidepsin, a new cytotoxic macrolide from Spongia sp.
2. Total Synthesis and Structural Assignment of Spongidepsin through a Stereodivergent Ring-Closing-Metathesis Strategy
3. Assignment of Absolute Stereochemistry and Total Synthesis of (−)-Spongidepsin
4. SYNTHESIS AND UTILIZATION OF INDIUM (I) IODIDE FOR IN SITU FORMATION OF ENANTIOENRICHED ALLENYLINDIUM REAGENTS AND THEIR ADDITION TO ALDEHYDES: (2R,3S,4S)-1-(tert-BUTYLDIPHENYLSILYLOXY)-2,4-DIMETHYL-5-HEXYN-3-OL
5. Effects of Olefin Geometry on the Stereochemistry of Lewis Acid Mediated Additions of Crotylstannanes to Aldehydes
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