ePrints@IIScePrints@IISc Home | About | Browse | Latest Additions | Advanced Search | Contact | Help

A New Tetrahydrofurannulation Via Tandem Radical Cyclization Reaction-Reductive Deoxygenation Sequence

Srikrishna, A and Viswajanani, R and Yelamaggad, CV (1995) A New Tetrahydrofurannulation Via Tandem Radical Cyclization Reaction-Reductive Deoxygenation Sequence. In: Tetrahedron Letters, 36 (7). pp. 1127-1128.

[img] PDF
1.pdf - Published Version
Restricted to Registered users only

Download (122Kb) | Request a copy
Official URL: http://www.sciencedirect.com/science?_ob=MImg&_ima...

Abstract

Treatment of bromoketals 2, derived from allyl alcohols 1, with tributyltin chloride, sodium cyanoborohydride and AIBN furnishes the tetrahydrofurannulated products 3 via a 5-exo-trig radical cyclisation reaction followed by reductive cleavage of ketal 4.

Item Type: Journal Article
Additional Information: Copyright of this article belongs to Elsavier.
Department/Centre: Division of Chemical Sciences > Organic Chemistry
Date Deposited: 02 Apr 2009 05:27
Last Modified: 19 Sep 2010 05:27
URI: http://eprints.iisc.ernet.in/id/eprint/19260

Actions (login required)

View Item View Item