Electronic control of the stereoselectivities of electrocyclic reactions of cyclobutenes against incredible steric odds

K.N. Houk; David C. Spellmeyer; Charles W. Jefford; C.G. Rimbault; Ying Wang; R.D. Miller

doi:10.1021/jo00244a058

Journal of Organic Chemistry

Paper

01 May 2002

Electronic control of the stereoselectivities of electrocyclic reactions of cyclobutenes against incredible steric odds

View publication

Abstract

Experimental studies of the electrocyclic reactions of 2- and 3-tert-butyl-3-(trimethylsiloxy)cyclobutene and of 3-methoxy-3-fert-butylcyclobutene confirm ab initio computational predictions. © 1988, American Chemical Society. All rights reserved.

Paper

Influence of basis sets and electron correlation on theoretically predicted infrared intensities

Paper

Experimental and Theoretical Studies of Substituent Effects on an Orbital Symmetry Forbidden Electrocyclization

Paper

Theoretical investigations of the rotational barrier in anisole: An ab initio and molecular dynamics study

Paper

Experimental and Theoretical Studies of Substituent Effects on an Orbital Symmetry Forbidden Electrocyclization

View all publications

Abstract

Related

Influence of basis sets and electron correlation on theoretically predicted infrared intensities

Experimental and Theoretical Studies of Substituent Effects on an Orbital Symmetry Forbidden Electrocyclization

Theoretical investigations of the rotational barrier in anisole: An ab initio and molecular dynamics study

Experimental and Theoretical Studies of Substituent Effects on an Orbital Symmetry Forbidden Electrocyclization