Transition-Metal-Free In Situ Generation of Terminal Alkenes: Synthesis of Multisubstituted Acrylamidines via Tandem sp3 C–H Olefination/sp2 C–H Arylation Reactions-Reference-Cited by-同舟云学术

Transition-Metal-Free In Situ Generation of Terminal Alkenes: Synthesis of Multisubstituted Acrylamidines via Tandem sp3 C–H Olefination/sp2 C–H Arylation Reactions

Published:2017-10-17 Issue:11 Volume:7 Page:7783-7787
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Pothikumar Rajagopal¹,Sujatha Chandragiri¹,Namitharan Kayambu¹²^ORCID

Affiliation:

1. Organic Synthesis and Catalysis Laboratory, SRM Research Institute, SRM University, Chennai 603203, India

2. Department of Chemistry, SRM University-AP, Amaravati 522502, India

Funder

Department of Science and Technology, Ministry of Science and Technology

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.7b02819

Reference48 articles.

1. Wang, J.Topics in Current Chemistry, Stereoselective Alkene Synthesis;Springer:Berlin, 2012; p327.

2. The Heck Reaction as a Sharpening Stone of Palladium Catalysis

3. The Asymmetric Intramolecular Heck Reaction in Natural Product Total Synthesis

4. Palladium-Catalyzed Cross-Coupling of α-Diazocarbonyl Compounds with Arylboronic Acids

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