Asymmetric Nitrene Transfer Reactions: Sulfimidation, Aziridination and C-H Amination Using Azide Compounds as Nitrene Precursors-Reference-Cited by-同舟云学术

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Asymmetric Nitrene Transfer Reactions: Sulfimidation, Aziridination and C-H Amination Using Azide Compounds as Nitrene Precursors

Published:2014-01-22 Issue:1 Volume:14 Page:117-129
ISSN:1527-8999
Container-title:The Chemical Record
language:en
Short-container-title:The Chemical Record

Author:

Uchida Tatsuya¹²,Katsuki Tsutomu²³

Affiliation:

1. Faculty of Arts and Science; Kyushu University; Hakozaki, Higashi-ku Fukuoka 812-8581 Japan

2. International Institute for Carbon-Neutral Energy Research (WPI-I2CNER); Kyushu University; Hakozaki, Higashi-ku Fukuoka 812-8581 Japan

3. Institute for Advanced Study; Kyushu University; Hakozaki, Higashi-ku Fukuoka 812-8581 Japan

Publisher

Wiley

Subject

Materials Chemistry,General Chemical Engineering,Biochemistry,General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/tcr.201300027/fullpdf

Reference122 articles.

1. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations

2. Enantioselective Catalytic Aziridinations and Asymmetric Nitrene Insertions into CH Bonds

3. Recent developments in asymmetric aziridination

4. Transition-metal-catalyzed aminations and aziridinations of CH and CC bonds with iminoiodinanes

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