Solvent reduced wittig olefination reactions with halo containing conjugated phosphoranes
Author:
Affiliation:
1. 1Institute of Materials Chemistry and Engineering, Kyushu University, Kasuyga-shi, Fukuoka, 816-8580, Japan
Abstract
Publisher
Walter de Gruyter GmbH
Subject
Materials Chemistry,General Chemistry
Link
http://link.springer.com/content/pdf/10.2478/s11532-006-0024-2.pdf
Reference65 articles.
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3. T. Thiemann, D. Ohira, Y.Q. Li, T. Sawada, S. Mataka, K. Rauch, M. Noltemeyer and A. de Meijere: “[4 + 2] Cycloaddition of thiophene S-monoxides to activated methylenecyclopropanes”, J. Chem. Soc., Perkin Trans. 1, (2000), pp. 2968–2976.
4. J.-P. Surivet, J.-N. Volle and J.M. Vatèle: “Easy access to an enantiopure precursor of (+)-goniodiol”, Tetrahedron: Asymmetry, Vol. 7, (1996), pp. 3305–3308.
5. C. Rüchardt, P. Panse and S. Eichler: “Mechanism of the Wittig reaction with triarylalkoxycarbonylmethylene phosphoranes”, Chem. Ber., Vol. 100, (1967), pp. 1144–1164
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