Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted α-hydroxy-β-amino amides-Reference-Cited by-同舟云学术

Carbamoyl anion-initiated cascade reaction for stereoselective synthesis of substituted α-hydroxy-β-amino amides

Published:2016 Issue:5 Volume:52 Page:912-915
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Lin Chao-Yang¹²³⁴⁵,Ma Peng-Ju¹²³⁴⁵,Sun Zhao⁶⁷⁸⁵,Lu Chong-Dao¹²³⁴⁵,Xu Yan-Jun¹²³⁴⁵

Affiliation:

1. The Key Laboratory of Plant Resources and Chemistry of Arid Zones

2. Xinjiang Technical Institute of Physics & Chemistry

3. Chinese Academy of Sciences

4. Urumqi 830011

5. China

6. Department of Chemistry and Applied Chemistry

7. Changji University

8. Changji 831100

Abstract

A carbamoyl anion-initiated cascade reaction with acylsilanes and imines allows rapid construction of substituted α-hydroxy-β-amino amides in high yields with excellent diastereoselectivities.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2016/CC/C5CC08118A

Reference53 articles.

1. Molecular rearrangements of organosilicon compounds

2. Synthesis and chemistry of acyl silanes

3. The Brook rearrangement in tandem bond formation strategies

4. Silyl Glyoxylates. Conception and Realization of Flexible Conjunctive Reagents for Multicomponent Coupling

5. Stereocontrolled Formation of Several Carbon–Carbon Bonds in Acyclic Systems

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