Configuration of the Major Stereoisomer of Zn/AcOH Reduction Product of 4-oxo-4H-chromene-3-carbaldehyde-Reference-Cited by-同舟云学术

Configuration of the Major Stereoisomer of Zn/AcOH Reduction Product of 4-oxo-4H-chromene-3-carbaldehyde

Published:2007-02 Issue:2 Volume:2007 Page:89-90
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Dey Sankar P.¹,Dey Dilip K.²,Mallik Asok K.³,Dahlenburg Lutz⁴

Affiliation:

1. Department of Chemistry, Srikrishna College, Bagula-741502, Nadia, West Bengal, India.

2. Department of Chemistry, Chandidas Mahavidyalaya, Khujutipara – 731215, Birbhum, West Bengal, India.

3. Department of Chemistry, Jadavpur University, Kolkata – 700032, West Bengal, India.

4. Institut für Anorganische Chemie, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstrasse 1, D-91058 Erlangen, Germany.

Abstract

Under modified Clemmensen reduction condition 4-oxo-4H-chromene-3-carbaldehyde gave two 1,2-diol products of which the configuration of the major diol was determined by X-ray crystallography

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/030823407X198294

Reference19 articles.

1. Selective tin and zinc mediated allylations of carbonyl compounds in aqueous media

2. Allylzinc reagents additions in aqueous media

3. Selective allylation of carbonyl compounds in aqueous media

4. Synthesis of homoallylic alcohols in aqueous media

5. A new method for coupling aromatic aldehydes and ketones to produce .alpha.-glycols using zinc-zinc dichloride in aqueous solution and in the solid state

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