(Bromodimethyl)sulfonium Bromide–Mediated Thiolysis of Epoxides: An Easy Access to β-Hydroxy Sulfides and Benzoxathiepinones in Solvent-Free Conditions-Reference-Cited by-同舟云学术

(Bromodimethyl)sulfonium Bromide–Mediated Thiolysis of Epoxides: An Easy Access to β-Hydroxy Sulfides and Benzoxathiepinones in Solvent-Free Conditions

Published:2010-11-16 Issue:24 Volume:40 Page:3629-3639
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Shailaja M.,Manjula A.,Vittal Rao B.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397910903458595

Reference39 articles.

1. Solvent‐free Organic Synthesis

2. Synthetic methods are reactions. 73. Conversion of epoxides and enamines into α-haloketones with halodimethylsulfonium halides

3. Efficient (bromodimethyl)sulfonium bromide mediated synthesis of benzimidazoles

4. (Bromodimethyl)sulfonium bromide: an inexpensive reagent for the solvent-free, one-pot synthesis of α-aminophosphonates

5. (Bromodimethyl)sulfonium bromide mediated Michael addition of thiols to α, β-unsaturated ketones

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