Literature DB >> 11348183

A novel and efficient methodology for the C-C bond forming radical cyclization of hydrophobic substrates in water.

Y Kita1, H Nambu, N G Ramesh, G Anilkumar, M Matsugi.   

Abstract

[reaction: see text]. The combination of water-soluble radical initiator 2,2'-azobis[2-(2-imidazolin-2-yl)propane] (VA-061), water-soluble chain carrier 1-ethylpiperidine hypophosphite (EPHP), and surfactant cetyltrimethylammonium bromide (CTAB) was found to be the most suitable condition for effective radical cyclization in water for a variety of hydrophobic substrates.

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Year:  2001        PMID： 11348183     DOI： 10.1021/ol010014p

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  2 in total

1.  Practical radical cyclizations with arylboronic acids and trifluoroborates.

Authors:  Jonathan W Lockner; Darryl D Dixon; Rune Risgaard; Phil S Baran
Journal:  Org Lett       Date:  2011-09-16       Impact factor: 6.005

2.  Microwave assisted convenient one-pot synthesis of coumarin derivatives via Pechmann condensation catalyzed by FeF3 under solvent-free conditions and antimicrobial activities of the products.

Authors:  Vahid Vahabi; Farhad Hatamjafari
Journal:  Molecules       Date:  2014-08-26       Impact factor: 4.411
  2 in total

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