Useful Synthesis of Fragment A–C–D of a Thiostrepton-type Macrocyclic Antibiotic, Thiocilline I

Useful synthesis of the main Fragment A–C–D segment constructing a thiostrepton-type macrocyclic antibiotic, thiocilline I, was first achieved by coupling of the 2,3,6-polythiazolesubstituted pyridine skeleton (Fragment A–C) with Fragment D.

Saved in:
Bibliographic Details
Published in:Chemistry letters 2004-07, Vol.33 (7), p.814-815
Main Authors: Suzuki, Shuusuke, Yonezawa, Yasuchika, Shin, Chung-gi
Format: Article
Language:English
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Useful synthesis of the main Fragment A–C–D segment constructing a thiostrepton-type macrocyclic antibiotic, thiocilline I, was first achieved by coupling of the 2,3,6-polythiazolesubstituted pyridine skeleton (Fragment A–C) with Fragment D.
ISSN:0366-7022
1348-0715
DOI:10.1246/cl.2004.814