Palladium(II)‐Catalyzed Sequential Aminopalladation and Oxidative Coupling with Acetylenes/Enones: Synthesis of Newly Substituted Quinolines from 2‐Aminophenyl Propargyl Alcohols-Reference-Cited by-同舟云学术

Palladium(II)‐Catalyzed Sequential Aminopalladation and Oxidative Coupling with Acetylenes/Enones: Synthesis of Newly Substituted Quinolines from 2‐Aminophenyl Propargyl Alcohols

Published:2015-12-22 Issue:2 Volume:358 Page:303-313
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Thirupathi Nuligonda¹,Puri Surendra¹,Reddy Thota Jagadeshwar²,Sridhar Balasubramanian³,Reddy Maddi Sridhar¹⁴

Affiliation:

1. Medicinal & Process Chemistry Division, CSIR‐Central Drug Research Institute, Lucknow, 226031, India

2. SAIF‐Division, CSIR‐Central Drug Research Institute, Lucknow, 226031, India

3. Dr. B. Sridhar, X‐Ray Crystallography Division, CSIR‐IICT, Tarnaka, Hyderabad, 500007, India

4. Academy of Scientific and Innovative Research, New Delhi 110001, India

Funder

DST

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.201500805

Reference107 articles.

2. 2,3-Disubstituted Indoles through the Palladium-Catalyzed Reaction of Aryl Chlorides witho-Alkynyltrifluoroacetanilides

3. Heck reaction of arenediazonium salts with N,N-diprotected allylamines. Synthesis of cinnamylamines and indoles

4. Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions

5. Preparation of 2,5-Disubstituted Oxazoles from N-Propargylamides

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