Synthesis 2015; 47(18): 2860-2868
DOI: 10.1055/s-0034-1378739
paper
© Georg Thieme Verlag Stuttgart · New York

Studies toward the Total Synthesis of Tianchimycins A and B: Construction of the Complete C1–C16 Framework

Sandeep AnkiReddy
Natural Products Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad-500 007, India   Email: gowravaramsr@yahoo.com   Email: sabitha@iict.res.in
,
Praveen AnkiReddy
Natural Products Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad-500 007, India   Email: gowravaramsr@yahoo.com   Email: sabitha@iict.res.in
,
Gowravaram Sabitha*
Natural Products Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad-500 007, India   Email: gowravaramsr@yahoo.com   Email: sabitha@iict.res.in
› Author Affiliations
Further Information

Publication History

Received: 12 March 2015

Accepted after revision: 28 April 2015

Publication Date:
25 June 2015 (online)


Abstract

A stereoselective synthesis of the complete C1–C16 framework of tianchimycins A and B is described. Key transformations include Horner–Wadsworth–Emmons, Evans aldol, Gilman’s and stereoselective alkylation reactions.

Supporting Information

 
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