The stereochemistry of nucleophilic addition to some conjugated cyclohexenes

C. W. Alexander; M. S. Hamdam; W. R. Jackson

doi:10.1039/C39720000094

The stereochemistry of nucleophilic addition to some conjugated cyclohexenes

C. W. Alexander, M. S. Hamdam, W. R. Jackson

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

7 Citations (Scopus)

Abstract

The products of axial attack have been found to predominate from two extreme types of nucleophilic addition reactions to conformationally rigid cyclohexenes.

Original language	English
Pages (from-to)	94-95
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Volume	0
Issue number	2
DOIs	https://doi.org/10.1039/C39720000094
Publication status	Published - 1 Dec 1972
Externally published	Yes

Access to Document

10.1039/C39720000094

Cite this

@article{30a1caa19621420284b739aa86bd9e7a,

title = "The stereochemistry of nucleophilic addition to some conjugated cyclohexenes",

abstract = "The products of axial attack have been found to predominate from two extreme types of nucleophilic addition reactions to conformationally rigid cyclohexenes.",

author = "Alexander, {C. W.} and Hamdam, {M. S.} and Jackson, {W. R.}",

year = "1972",

month = dec,

day = "1",

doi = "10.1039/C39720000094",

language = "English",

volume = "0",

pages = "94--95",

journal = "Journal of the Chemical Society, Chemical Communications",

issn = "0022-4936",

publisher = "The Royal Society of Chemistry",

number = "2",

}

TY - JOUR

T1 - The stereochemistry of nucleophilic addition to some conjugated cyclohexenes

AU - Alexander, C. W.

AU - Hamdam, M. S.

AU - Jackson, W. R.

PY - 1972/12/1

Y1 - 1972/12/1

N2 - The products of axial attack have been found to predominate from two extreme types of nucleophilic addition reactions to conformationally rigid cyclohexenes.

AB - The products of axial attack have been found to predominate from two extreme types of nucleophilic addition reactions to conformationally rigid cyclohexenes.

UR - http://www.scopus.com/inward/record.url?scp=37049117049&partnerID=8YFLogxK

U2 - 10.1039/C39720000094

DO - 10.1039/C39720000094

M3 - Article

AN - SCOPUS:37049117049

SN - 0022-4936

VL - 0

SP - 94

EP - 95

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 2

ER -

The stereochemistry of nucleophilic addition to some conjugated cyclohexenes

Abstract

Access to Document

Other files and links

Cite this