How To Achieve High Regioselectivity in Barrier-less Nucleophilic Addition to p-Benzynes Generated via Bergman Cyclization of Unsymmetrical Cyclic Azaenediyne?-Reference-Cited by-同舟云学术

How To Achieve High Regioselectivity in Barrier-less Nucleophilic Addition to p-Benzynes Generated via Bergman Cyclization of Unsymmetrical Cyclic Azaenediyne?

Published:2019-01-28 Issue:5 Volume:84 Page:2911-2921
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Das Eshani¹,Basak Shyam¹,Anoop Anakuthil¹^ORCID,Chand Santanu¹,Basak Amit¹^ORCID

Affiliation:

1. Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721 302, India

Funder

Science and Engineering Research Board

Indian Institute of Technology Kharagpur

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b00060

Reference44 articles.

1. Calichemicins, a novel family of antitumor antibiotics. 1. Chemistry and partial structure of calichemicin .gamma.1I

2. Calichemicins, a novel family of antitumor antibiotics. 2. Chemistry and structure of calichemicin .gamma.1I

3. Esperamicins, a novel class of potent antitumor antibiotics. 2. Structure of esperamicin X

4. Chemistry and Biology of the Enediyne Anticancer Antibiotics

5. An acyclic enediyne anticancer compound attributed to a Bergman cyclization at physiological temperature

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