Microwave-Assisted Solvent-Free Synthesis of (E)-Stilbenes-Reference-Cited by-同舟云学术

Microwave-Assisted Solvent-Free Synthesis of (E)-Stilbenes

Published:2012-04 Issue:4 Volume:36 Page:231-234
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Wang Liu-chang¹,Li Jiang¹,Zhang Xi-quan²,Gu Hong-mei²,Li Bao-lin¹

Affiliation:

1. Key Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry, and School of Chemistry & Chemical Engineering, Shaanxi Normal University, Xi'an 710062, P. R. China

2. Jiangsu Chia Tai Tianqing Pharmaceutical Co., Ltd. Nanjing 210042, P. R. China

Abstract

An efficient synthesis of a series of stilbenes is reported using 4-nitrotoluene and substituted arylaldehydes as starting materials in the presence of Cs2CO3 and polyethylene glycol under solvent-free microwave irradiation. Compared with conventional method, this strategy exhibited higher stereoselectivity, shorter reaction times and has a lower environmental impact.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/174751912X13320888894748

Reference34 articles.

1. Resveratrol and its analogs: Defense against cancer, coronary disease and neurodegenerative maladies or just a fad?

2. Therapeutic potential of resveratrol: the in vivo evidence

3. Comparison of the fungicidal activities of (E)-4-hydroxylated stilbenes and related bibenzyls

4. Role of stilbenes in the natural durability of wood: Fungicidal structure-activity relationships

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