A Facile and Convenient Synthesis of Trisubstituted (E)-α,β-Unsaturated Esters by Tandem Acetylation-E1cB Reaction.
E1cB reaction
stereoselective synthesis
tandem acetylation-E1cB reaction
trisubstituted (E)-α,β-unsaturated ester
Journal
Chemical & pharmaceutical bulletin
ISSN: 1347-5223
Titre abrégé: Chem Pharm Bull (Tokyo)
Pays: Japan
ID NLM: 0377775
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
5
1
2019
pubmed:
5
1
2019
medline:
14
2
2019
Statut:
ppublish
Résumé
A facile and convenient synthesis of trisubstituted (E)-α,β-unsaturated esters was developed by improving our previously established method. The new method circumvented the separation of the intermediates, which have an activating group of the hydroxyl group in β-hydroxy esters, furnishing α,β-unsaturated esters in shorter steps than the previous method: an acetylation of β-hydroxy group and subsequent E1cB reaction proceeded in tandem. In addition, the new method can not only employ a diastereomeric mixture of the substrate for the E1cB reaction, it has a wide substrate scope as well, which would enable the synthesis of various trisubstituted (E)-α,β-unsaturated esters.
Identifiants
pubmed: 30606952
doi: 10.1248/cpb.c18-00666
doi:
Substances chimiques
Esters
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM