Issue 1, 1978
From the journal:

Journal of the Chemical Society, Chemical Communications

Stereochemistry of the adduct from t-butylcyanoketen and 2-methylbut-2-ene; X-ray crystal and molecular structure of 2-cyano-3,3,4-trimethyl-2-t-butylcyclobutyl p-chlorobenzoate

Peter R. Brook,   Afaf M. Eldeeb,   Keith Hunt  and  Walter S. McDonald  

Abstract

Cycloaddition of t-butylcyanoketen and 2-methylbut-2-ene proceeds regio- and stereo-specifically to give the cyclobutanone (1) whose structure is deduced by X-ray crystallography of the 4-chlorobenzoate of the derived alcohol (2).

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Article information

DOI
https://doi.org/10.1039/C39780000010
Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 10-11

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Stereochemistry of the adduct from t-butylcyanoketen and 2-methylbut-2-ene; X-ray crystal and molecular structure of 2-cyano-3,3,4-trimethyl-2-t-butylcyclobutyl p-chlorobenzoate

P. R. Brook, A. M. Eldeeb, K. Hunt and W. S. McDonald, J. Chem. Soc., Chem. Commun., 1978, 10 DOI: 10.1039/C39780000010

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