Rate acceleration of the Baylis-Hillman reaction using crystalline cyclodextrin complexes

DOI: 10.1080/00304940009356284

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Organic Preparations and Procedures International p. 185 - 203 (2000)

Update date:2022-08-17

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Authors:

Reddy, L. Rajender

Rao, K. Rama

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Article abstract of DOI:10.1080/00304940009356284

Full text of DOI:10.1080/00304940009356284

Organic Preparations and Procedures International

ISSN: 0030-4948 (Print) 1945-5453 (Online) Journal homepage: http://www.tandfonline.com/loi/uopp20

RATE ACCELERATION OF THE BAYLIS-HILLMAN

REACTION USING CRYSTALLINE CYCLODEXTRIN

COMPLEXES

L. Rajender Reddy & K. Rama Rao

To cite this article: L. Rajender Reddy & K. Rama Rao (2000) RATE ACCELERATION OF THE

BAYLIS-HILLMAN REACTION USING CRYSTALLINE CYCLODEXTRIN COMPLEXES, Organic

Preparations and Procedures International, 32:2, 185-188, DOI: 10.1080/00304940009356284

To link to this article: http://dx.doi.org/10.1080/00304940009356284

Published online: 12 Feb 2009.

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Article Doi

Rate acceleration of the Baylis-Hillman reaction using crystalline cyclodextrin complexes

DOI: 10.1080/00304940009356284

Source and publish data:

Authors:

Article abstract of DOI:10.1080/00304940009356284

Full text of DOI:10.1080/00304940009356284

Products guided by the article

R&D Labs maybe for 109022-85-7

Relevant to this article

Multicomponent Synthesis of Unsymmetrical 4,5-Disubstituted Imidazolium Salts as N-Heterocyclic Carbene Precursors: Applications in Palladium-Catalyzed Cross-Coupling Reactions

New utility of electrophilic trifluoromethylthiolation reagents for the synthesis of a variety of triflones

Chemically triggered C-ON bond homolysis in alkoxyamines: Regioselectivity and chemoselectivity

Crystal structure of tryptophan lyase (NosL): Evidence for radical formation at the amino group of tryptophan