One-pot synthesis of 3,5-disubstituted and polysubstituted phenols from acyclic precursors

A new strategy for the synthesis of 3,5-disubstituted phenols is established through one-pot Robinson annulation of α,β-unsaturated ketones with α-fluoro-β-ketoesters followed by in situ dehydrofluorination and tautomerization. This method has been extended to the synthesis of polysubstituted phenols and applied in the preparation of biologically active compounds.

Medienart:

E-Artikel

Erscheinungsjahr:

2015

Erschienen:

2015

Enthalten in:

Zur Gesamtaufnahme - volume:17

Enthalten in:

Organic letters - 17(2015), 5 vom: 06. März, Seite 1090-3

Sprache:

Englisch

Beteiligte Personen:

Qian, Jinlong [VerfasserIn]
Yi, Wenbin [VerfasserIn]
Huang, Xin [VerfasserIn]
Miao, Yongbo [VerfasserIn]
Zhang, Junkai [VerfasserIn]
Cai, Chun [VerfasserIn]
Zhang, Wei [VerfasserIn]

Links:

Volltext

Themen:

Esters
Journal Article
Ketones
Phenols
Research Support, Non-U.S. Gov't

Anmerkungen:

Date Completed 31.08.2015

Date Revised 06.03.2015

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1021/ol503615n

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM246172924