A convenient one-pot completely stereoselective synthesis of trans-4-hydroxystilbenes and its derivatives and X-ray structure of its precursor

Chhor, Rakeshwar B. and Singh, Kunwar A. and Nosse, B. and Tandon, Vishnu K. (2003) A convenient one-pot completely stereoselective synthesis of trans-4-hydroxystilbenes and its derivatives and X-ray structure of its precursor. SYNTHETIC COMMUNICATIONS, 33 (14). pp. 2519-2530. ISSN 0039-7911, 1532-2432

Full text not available from this repository. (Request a copy)

Abstract

The synthesis of E-isomer of 4-Hydroxystilbene and its derivatives 3 by reductive elimination of the carbonyl function in 2-phenyl-1-(4-hydroxyphenyl)ethan-1-one and its derivatives 2 and the X-ray structure of 2a are described.

Item Type: Article
Uncontrolled Keywords: INHIBITORS; POLYMERS; STILBENE; TRANS; stereoselective; trans-4-hydroxystilbene; reductive elimination; X-ray structure; fries rearrangement
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Organische Chemie
Depositing User: Dr. Gernot Deinzer
Date Deposited: 05 Aug 2021 10:54
Last Modified: 05 Aug 2021 10:54
URI: https://pred.uni-regensburg.de/id/eprint/39545

Actions (login required)

View Item View Item