In:
European Journal of Organic Chemistry, Wiley, Vol. 2007, No. 28 ( 2007-10), p. 4758-4764
Abstract:
A new series of conformationally locked N,O‐nucleoside analogues was synthesized by exploiting allenic nucleobases as dipolarophiles in 1,3‐dipolar nitrone cycloadditions. The regio‐ and sitoselectivity of the reaction were rationalized according to the frontier orbital treatment of the nitrone cycloaddition by AM1 calculations. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)
Type of Medium:
Online Resource
ISSN:
1434-193X
,
1099-0690
DOI:
10.1002/ejoc.v2007:28
DOI:
10.1002/ejoc.200700171
Language:
English
Publisher:
Wiley
Publication Date:
2007
detail.hit.zdb_id:
1475010-7
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