Synthesis, in vitro antiproliferative activity, antioxidant activity and molecular modeling studies of new carbazole Mannich bases-Reference-Cited by-同舟云学术

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Synthesis, in vitro antiproliferative activity, antioxidant activity and molecular modeling studies of new carbazole Mannich bases

Published:2017-05-29 Issue:10 Volume:26 Page:2243-2259
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Narayana Reddy Pedavenkatagari,Padmaja Pannala,Ramana Reddy Bobbala,Singh Jadav Surender

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/article/10.1007/s00044-017-1927-5/fulltext.html

Reference73 articles.

1. Alden-Danforth E, Scerba MT, Lectka T (2008) Asymmetric cycloadditions of o-quinone methides employing chiral ammonium. Org Lett 10(21):4951–4953

2. Amouri H, Bras JL (2002) Taming reactive phenol tautomers and o-quinone methides with transition metals: a structure-reactivity relationship. Acc Chem Res 35(7):501–510

3. Bai WJ, David JG, Feng ZG, Weaver MG, Wu K, Pettus TRR (2014) The domestication of ortho-quinone methides. Acc Chem Res 47(12):3655–3664

4. Balasubramanian KK, Selvaraj S (1980) Novel reaction of o-phenolic mannich bases with alpha-chloroacrylonitrile. J Org Chem 45(18):3726–3727

5. Basaric N, Majerski KM, Kralj M (2014) Quinone methides: photochemical generation and its application in biomedicine. Curr Org Chem 18(1):3–18

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