Direct Synthesis of N -Acyl-N ,O -hemiacetals via Nucleophilic Addition of Unactivated Amides and Their O -Acetylation: Access to α,α-Difunctionalized N -Acylimines-Reference-Cited by-同舟云学术

Direct Synthesis of N -Acyl-N ,O -hemiacetals via Nucleophilic Addition of Unactivated Amides and Their O -Acetylation: Access to α,α-Difunctionalized N -Acylimines

Published:2016-08-03 Issue:17 Volume:358 Page:2817-2828
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Asahara Haruyasu¹²,Inoue Kanami¹,Tani Shinki³,Umezu Kazuto³,Nishiwaki Nagatoshi¹²

Affiliation:

1. School of Environmental Science and Engineering; Kochi University of Technology; Kami, Kochi 782-8502 Japan,

2. Research Center for Material Science and Engineering; Kochi University of Technology; Kami, Kochi 782-8502 Japan

3. Marketing & Development Department; Ihara Chemical Industry Co., Ltd.; Fujikawa-cho, Ihara-gun, Shizuoka 421-3306 Japan

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/adsc.201600436/fullpdf

Reference59 articles.

1. α-Amido Sulfones as Stable Precursors of Reactive N-Acylimino Derivatives

2. Benzotriazole mediated amino-, amido-, alkoxy- and alkylthio-alkylation

3. Recent Advances in Stereoselective Syntheses Using N-Acylimines

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