Unusual dimerization of N-protected bromomethylindoles/benzyl bromide with arylmetal halides: generation of indolylmethyl/benzyl radical-Reference-Cited by-同舟云学术

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Unusual dimerization of N-protected bromomethylindoles/benzyl bromide with arylmetal halides: generation of indolylmethyl/benzyl radical

Published:2008-02 Issue:9 Volume:64 Page:2071-2079
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Ramesh Neelamegam,Prakash Chandran,Sureshbabu Radhakrishnan,Dhayalan Vasudevan,Mohanakrishnan Arasambattu K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference30 articles.

1. Dichlorocarbene-induced deamination of naphthalen-1,4-imines and anthracen-9,10-imines

2. Synthesis and Diels-Alder reactions of 1,3-dimethyl-4-(phenylsulfonyl)-4H-furo[3,4-b]indole. A new annulation strategy for the construction of ellipticine and isoellipticine

3. Total syntheses of ellipticine alkaloids and their amino analogues

4. A Simple Synthesis of 2-Substituted Indoles

5. A Versatile Construction of the 8H-Quino[4,3-b]carbazole Ring System as a Potential DNA Binder

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3. Ni(II)-Catalyzed Oxidative Coupling of Arenes;Chinese Journal of Organic Chemistry;2020

4. 3.07 Coupling Reactions Between sp3-Carbon Centers;Comprehensive Organic Synthesis II;2014

5. Experimental;Selectivity in the Synthesis of Cyclic Sulfonamides;2014

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