Stereoselective total synthesis of atpenins a4 and b, harzianopyridone, and NBRI23477 B.

Chem Pharm Bull (Tokyo)

Graduate School of Pharmaceutical Sciences, Kitasato University, 5–9–1 Shirokane, Minato-ku, Tokyo, Japan.

Published: November 2012

The stereoselective total synthesis of atpenins A4 (2) and B (3), harzianopyridone (4), and NBRI23477 B (5) have been developed using a convergent approach involving the coupling reaction of a common iodopyridine with an aldehyde corresponding to the appropriate side chain of the desired compound. Furthermore, the absolute configurations of atpenin B (3), harzianopyridone (4), and NBRI23477 B (5) have been unambiguously determined.

Download full-text PDF

Source
http://dx.doi.org/10.1248/cpb.c12-00266DOI Listing

Publication Analysis

Top Keywords

harzianopyridone nbri23477
12
stereoselective total
8
total synthesis
8
synthesis atpenins
8
atpenins harzianopyridone
8
nbri23477 stereoselective
4
nbri23477 developed
4
developed convergent
4
convergent approach
4
approach involving
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!