The ene reaction of 5-allyl-2ϵ-hydroxy-5α-cholestan-3-one: An unusually facile ene reaction

Brian A. Marples; Christopher D. Spilling

doi:10.1016/S0040-4039(00)95787-3

The ene reaction of 5-allyl-2ϵ-hydroxy-5α-cholestan-3-one: An unusually facile ene reaction

Brian A. Marples, Christopher D. Spilling

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

Original language	American English
Journal	Tetrahedron Letters
Volume	28
DOIs	https://doi.org/10.1016/S0040-4039(00)95787-3
State	Published - Jan 1 1987
Externally published	Yes

Disciplines

Organic Chemistry
Chemistry

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title = "The ene reaction of 5-allyl-2ϵ-hydroxy-5α-cholestan-3-one: An unusually facile ene reaction",

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

note = "The ene reaction of the unsaturated acyloins (8) occurs smoothly at 110°C demonstrating the greater reactivity of the acyloin versus the analogous ket...",

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doi = "10.1016/S0040-4039(00)95787-3",

language = "American English",

volume = "28",

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T1 - The ene reaction of 5-allyl-2ϵ-hydroxy-5α-cholestan-3-one: An unusually facile ene reaction

AU - Marples, Brian A.

AU - Spilling, Christopher D.

N1 - The ene reaction of the unsaturated acyloins (8) occurs smoothly at 110°C demonstrating the greater reactivity of the acyloin versus the analogous ket...

PY - 1987/1/1

Y1 - 1987/1/1

UR - https://www.sciencedirect.com/science/article/pii/S0040403900957873

U2 - 10.1016/S0040-4039(00)95787-3

DO - 10.1016/S0040-4039(00)95787-3

M3 - Article

VL - 28

JO - Tetrahedron Letters

JF - Tetrahedron Letters

ER -

The ene reaction of 5-allyl-2ϵ-hydroxy-5α-cholestan-3-one: An unusually facile ene reaction

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