A new redundant rearrangement of aromatic ring fused cyclic α-hydroxydithiane derivatives. Synthesis of aromatic ring fused cyclic 1,2-diketones with one-carbon ring expansion

Ranu, Brindaban C. ; Jana, Umasish (1999) A new redundant rearrangement of aromatic ring fused cyclic α-hydroxydithiane derivatives. Synthesis of aromatic ring fused cyclic 1,2-diketones with one-carbon ring expansion The Journal of Organic Chemistry, 64 (17). pp. 6380-6386. ISSN 0022-3263

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Official URL: http://pubs.acs.org/doi/abs/10.1021/jo990634s

Related URL: http://dx.doi.org/10.1021/jo990634s

Abstract

A new reaction involving rearrangement of aromatic ring fused cyclic dithiane alcohol by N-chlorosuccinimide in CH2Cl2-H2O to the corresponding one-carbon ring expanded 1,2-diketone has been developed. A wide range of structurally varied dithiane alcohols have been found to undergo this rearrangement in high yields. The general criteria and reaction mechanism for this rearrangement have also been worked out.

Item Type:Article
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Deposited On:30 May 2011 04:57
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