The intramolecular ene reaction of 5-(prop-2-enyl)-2ξ-hydroxy- 5α-cholestan-3-one.

Brian A. Marples; Christopher D. Spilling

doi:10.1016/S0040-4020(01)89352-2

The intramolecular ene reaction of 5-(prop-2-enyl)-2ξ-hydroxy- 5α-cholestan-3-one.

Brian A. Marples, Christopher D. Spilling

Research output: Contribution to journal › Article › peer-review

Original language	American English
Journal	Tetrahedron
Volume	50
DOIs	https://doi.org/10.1016/S0040-4020(01)89352-2
State	Published - Jan 1 1994
Externally published	Yes

Disciplines

Organic Chemistry
Chemistry

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title = "The intramolecular ene reaction of 5-(prop-2-enyl)-2ξ-hydroxy- 5α-cholestan-3-one.",

author = "Marples, {Brian A.} and Spilling, {Christopher D.}",

note = "The title unsaturated acyloin undergoes the relatively low temperature (110°C) intramolecular ene reaction to give the 2,5-ethano-acyloin (17) which r...",

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doi = "10.1016/S0040-4020(01)89352-2",

language = "American English",

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T1 - The intramolecular ene reaction of 5-(prop-2-enyl)-2ξ-hydroxy- 5α-cholestan-3-one.

AU - Marples, Brian A.

AU - Spilling, Christopher D.

N1 - The title unsaturated acyloin undergoes the relatively low temperature (110°C) intramolecular ene reaction to give the 2,5-ethano-acyloin (17) which r...

PY - 1994/1/1

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UR - https://www.sciencedirect.com/science/article/pii/S0040402001893522

U2 - 10.1016/S0040-4020(01)89352-2

DO - 10.1016/S0040-4020(01)89352-2

M3 - Article

VL - 50

JO - Tetrahedron

JF - Tetrahedron

ER -

The intramolecular ene reaction of 5-(prop-2-enyl)-2ξ-hydroxy- 5α-cholestan-3-one.

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