Various difunctionalizations of acrylamide: an efficient approach to synthesize oxindoles-Reference-Cited by-同舟云学术

Various difunctionalizations of acrylamide: an efficient approach to synthesize oxindoles

Published:2016 Issue:19 Volume:14 Page:4365-4377
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Li Chen-Chen¹²³⁴⁵,Yang Shang-Dong¹²³⁴⁶

Affiliation:

1. State Key Laboratory of Applied Organic Chemistry

2. Lanzhou University

3. Lanzhou 730000

4. P. R. China

5. Cuiying Honors College

6. State Key Laboratory for Oxo Synthesis and Selective Oxidation

Abstract

In this review, we summarize the advancement and applications in the difunctionalization of acrylamide to synthesize oxindoles based on the mechanism.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB00554C

Reference160 articles.

1. Isatins As Privileged Molecules in Design and Synthesis of Spiro-Fused Cyclic Frameworks

2. Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones

3. The Palladium Catalyzed Asymmetric Addition of Oxindoles and Allenes: An Atom-Economical Versatile Method for the Construction of Chiral Indole Alkaloids

4. Gelsemine: A Thought-Provoking Target for Total Synthesis

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