## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Regioselectivity of a 1,3-dipolar cycloaddition to phenyl vinyl sulfoxide
β Scribed by Tyler C. Gray; Faraj Hasanayn; David P. Richardson; J. Hodge Markgraf
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 152 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.286
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β¦ Synopsis
Abstract
magnified image The regioselectivity of the 1,3βdipolar cycloaddition of benzonitrile Nβoxide to phenyl vinyl sulfoxide is established by isotopic labeling and ^13^C NMR analysis, and by DFT calculations. J. Heterocyclic Chem., (2009).
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Synthesis of a series of novel 1,3-diphenyl-4-arylspiropyrazolines[5.2 1 ]-1 1 -tetralones has been accomplished in good yield by regioselective 1,3dipolar cycloaddition of diphenylnitrilimine with (E)-2-arylidene-1-tetralones. X-ray crystal structure analysis of one of the products 4b confirms the
## Abstract Sulfonyl bis pyrazolines and isoxazolines were prepared by 1,3βdipolar cycloaddition of nitrile imines and nitrile oxides to E,Eβbis(styryl) sulfones. Β© 2002 Wiley Periodicals, Inc. Heteroatom Chem 13:677β682, 2002; Published online in Wiley InterScience (www.interscience.wiley.com). DO