Stereoselective Hydroboration of the 22(23)-Double Bond of Stigmasterol-like Side Chain: an Easy Approach to 22 and 23 Hydroxylated 24-Ethylsterols.

F Nicotra; Luigi PANZA; F Ronchetti; L. Toma

Stereoselective Hydroboration of the 22(23)-Double Bond of Stigmasterol-like Side Chain: an Easy Approach to 22 and 23 Hydroxylated 24-Ethylsterols.

F Nicotra, Luigi PANZA, F Ronchetti, L. Toma

Department of Pharmaceutical Sciences

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	649-651
Number of pages	3
Journal	Gazzetta Chimica Italiana
Volume	115
Publication status	Published - 1 Jan 1985

Cite this

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title = "Stereoselective Hydroboration of the 22(23)-Double Bond of Stigmasterol-like Side Chain: an Easy Approach to 22 and 23 Hydroxylated 24-Ethylsterols.",

author = "F Nicotra and Luigi PANZA and F Ronchetti and L. Toma",

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journal = "Gazzetta Chimica Italiana",

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T1 - Stereoselective Hydroboration of the 22(23)-Double Bond of Stigmasterol-like Side Chain: an Easy Approach to 22 and 23 Hydroxylated 24-Ethylsterols.

AU - Nicotra, F

AU - PANZA, Luigi

AU - Ronchetti, F

AU - Toma, L.

PY - 1985/1/1

Y1 - 1985/1/1

UR - https://iris.uniupo.it/handle/11579/2459

M3 - Article

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EP - 651

JO - Gazzetta Chimica Italiana

JF - Gazzetta Chimica Italiana

ER -

Stereoselective Hydroboration of the 22(23)-Double Bond of Stigmasterol-like Side Chain: an Easy Approach to 22 and 23 Hydroxylated 24-Ethylsterols.

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