Convenient synthesis of a central 2,3,6-trisubstituted pyridine skeleton of a macrobicyclic antibiotic, cyclothiazomycin

Authors
Okabe, A Ito, A Okumura, K Shin, C
Citation
A. Okabe et al., Convenient synthesis of a central 2,3,6-trisubstituted pyridine skeleton of a macrobicyclic antibiotic, cyclothiazomycin, CHEM LETT, (5), 2001, pp. 380-381
Citations number
5
Categorie Soggetti
Chemistry
Journal title
CHEMISTRY LETTERS
ISSN journal
03667022 → ACNP
Issue
5
Year of publication
2001
Pages
380 - 381
Database
ISI
SICI code
0366-7022(20010505):5<380:CSOAC2>2.0.ZU;2-R
Abstract
The first convenient synthesis of the main central 2,3,6-trisubstituted pyr idine skeleton [protected Fragment A-B] of a macrobicyclic antibiotic, cycl othiazomycin, was achieved.