Stereoselective synthesis of the C13–C22 fragment of callystatin A by a non-aldol approach
Author:
Affiliation:
1. Natural Product Chemistry Division
2. Indian Institute of Chemical Technology
3. Hyderabad 500007
4. India
Abstract
A stereoselective route to the C13–C22 subunit of callystatin A is disclosed.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB00413F
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1. The Chemistry and Biology of the Leptomycin Family
2. Antitumor activity of leptomycin B.
3. Callystatin A, a potent cytotoxic polyketide from the marine sponge, Callyspongia truncata
4. Absolute stereostructure of callystatin A, a potent cytotoxic polyketide from the marine sponge, Callyspongia truncata
5. Total synthesis of callystatin A, a potent cytotoxic polyketide from the marine sponge, Callyspongia truncata
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1. Regio- and Stereo-controlled Addition Reaction of Aminoallylic Stannanes to Aldehydes Mediated by Germanium Dichloride;Chemistry Letters;2018-07-05
2. Stereoselective total synthesis of (−)-nupharamine utilizing an α-chlorosulfide and a sulfinimine for C–C bond formation;Organic & Biomolecular Chemistry;2016
3. Stereoselective synthesis of the C1–C12 subunit of (−)-callystatin A;Tetrahedron Letters;2015-07
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