An iterative Shimizu non-aldol approach for the stereoselective synthesis of C13-C22 fragment of callystatin A

2012 ◽  
Vol 10 (9) ◽  
pp. 1750 ◽  
Author(s):  
Sandip A. Pujari ◽  
Krishna P. Kaliappan
Keyword(s):  
Stereoselective Synthesis ◽  
Callystatin A

Recent results toward the stereoselective synthesis of biologically active natural products

2007 ◽  
Vol 79 (2) ◽  
pp. 163-172 ◽  
Author(s):  
Luiz C. Dias ◽  
Luciana G. de Oliveira ◽  
Paulo R. R. Meira
Keyword(s):  
Natural Products ◽  
Total Synthesis ◽  
Cell Cultures ◽  
Stereoselective Synthesis ◽  
Animal Cell ◽  
Biologically Active ◽  
Asymmetric Total Synthesis ◽  
Callystatin A ◽  
Animal Cell Cultures ◽  
Active Natural

This paper describes the convergent and stereocontrolled asymmetric total synthesis of (+)-crocacins C and D, potent inhibitors of animal cell cultures and several yeasts and fungi, and (-)-callystatin A, a potent antitumor polyketide.

Stereoselective synthesis of the C13–C22 fragment of callystatin A by a non-aldol approach

2015 ◽  
Vol 13 (17) ◽  
pp. 5044-5053 ◽  
Author(s):  
Sadagopan Raghavan ◽  
Sheelamanthula Rajendar
Keyword(s):  
Stereoselective Synthesis ◽  
Callystatin A

A stereoselective route to the C13–C22 subunit of callystatin A is disclosed.

Stereoselective synthesis of the C1–C12 subunit of (−)-callystatin A

2015 ◽  
Vol 56 (29) ◽  
pp. 4371-4373 ◽  
Author(s):  
Sadagopan Raghavan ◽  
Sheelamanthula Rajendar
Keyword(s):  
Stereoselective Synthesis ◽  
Callystatin A
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