Design, synthesis, and diversification of 3,5-substituted enone library.

Abstract:

:This paper describes the synthesis of a 300 member library of 3,5-substituted enones. The synthesis starts with 6 different bromoenones that are accessed from the corresponding 1,3 diones. These bromides are then diversified by Suzuki coupling with a variety of aromatic and vinyl boronic acids. Additionally a small series of triazoles was synthesized by a Sonogashira coupling reaction dipolar cycloaddition sequence. The library was analyzed by principal component analysis to examine its diversity.

journal_name

ACS Comb Sci

authors

Khalaf J,Estrella-Jimenez ME,Shashack MJ,Phatak SS,Zhang S,Gilbertson SR

doi

10.1021/co200070m

subject

Has Abstract

pub_date

2011-07-11 00:00:00

pages

351-6

issue

4

eissn

2156-8952

issn

2156-8944

journal_volume

13

pub_type

信件
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