Synthesis of fluorinated chirons: Stereoselective oxirane formation by reaction of diazomethane on 1-fluoro-3-arylsulfinyl-2-propanone and ring opening by selected nucleophiles-Reference-Cited by-同舟云学术

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Synthesis of fluorinated chirons: Stereoselective oxirane formation by reaction of diazomethane on 1-fluoro-3-arylsulfinyl-2-propanone and ring opening by selected nucleophiles

Published:1995-07 Issue:30 Volume:51 Page:8289-8310
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Arnone Alberto,Bravo Pierfrancesco,Frigerio Massimo,Salani Giuliana,Viani Fiorenza,Zappalà Carmela,Cavicchio Giancarlo,Crucianelli Marcello

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference63 articles.

1. Recent advances in the preparation and synthetic applications of oxiranes

2. Synthetically Useful Reactions of Epoxides

3. Small Ring Heterocycles;Bartok,1985

4. Cyclic Sulfites and Cyclic Sulfates: Epoxide like Synthons

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3. Stereoselective Nucleophilic Fluoromethylation of Aryl Ketones: Dynamic Kinetic Resolution of Chiral α-Fluoro Carbanions;Angewandte Chemie;2013-12-04

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5. Epihalohydrins in Organic Synthesis;Chemical Reviews;2012-12-05

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