AIPO4 supported zinc borohydride as a novel reagent for the hydration of aromatic alkenes and alkynes

Article abstract of DOI:10.1080/00397919608002600

Hydration of aromatic alkenes (styrene, α-methylstyrene and E-stilbene) and alkynes (phenyl and diphenylacetylene) has been achieved by the reaction of the corresponding alkenes or alkynes or zinc borohydride combined with AIPO₄ in DME. Except in the case of α-methylstyrene, Zn(BH₄)₂/AIPO₄ provides a more efficient and selective catalytic system than the combination with SIO₂ or Al₂O₃.

Full text of DOI:10.1080/00397919608002600

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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AIPO4 Supported Zinc
Borohydride as a Novel Reagent
for the Hydration of Aromatic
Alkenes and Alkynes
Juan M. Campelo a , Rupak Chakraborty a & Jose M.
Marinas a
a Department of Organic Chemistry , University of
Cordoba Avda. S. Alberto Magno , E-14004, Córdoba,
Spain
Published online: 21 Aug 2006.
To cite this article: Juan M. Campelo , Rupak Chakraborty & Jose M. Marinas
(1996) AIPO4 Supported Zinc Borohydride as a Novel Reagent for the Hydration of
Aromatic Alkenes and Alkynes, Synthetic Communications: An International Journal
for Rapid Communication of Synthetic Organic Chemistry, 26:9, 1639-1650, DOI:
10.1080/00397919608002600
To link to this article: http://dx.doi.org/10.1080/00397919608002600
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