Cycloaddition of heterofunctionalized allenes withtert-butylthioacrylonitrile. Determination of activation parameters for diradical intermediate formation and the detection of reversible ring closure-Reference-Cited by-同舟云学术

Cycloaddition of heterofunctionalized allenes withtert-butylthioacrylonitrile. Determination of activation parameters for diradical intermediate formation and the detection of reversible ring closure

Published:1992-03 Issue:3 Volume:5 Page:160-170
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Pasto Daniel J.,Kong Wei

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference19 articles.

1. Cycloaddition of substituted allenes with 1,1-dichloro-2,2-difluoroethene. A model for the two-step, diradical-intermediate cycloaddition of allenes

2. Detection and the analysis of the factors affecting the competition between ring closure, internal rotation, and cleavage in diradical intermediates formed in allene cycloaddition reactions

3. Cycloaddition reactions of 1,3-dimethylallene. Assignment of stereochemistry of the cycloadducts and interpretation of product distributions

4. Stereochemical features of the (2 + 2) cycloaddition reactions of chiral allenes. 3. The cycloaddition of enantioenriched 1,3-dimethylallene with the symmetrically 1,1-disubstituted alkenes 1,1-dichloro-2,2-difluoroethene and 1,1-diphenylethene

5. and in Substituent Effects in Radical Chemistry, edited by and pp. 371-374. Reidel, Dordrecht (1986).

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Enantioselectivity of the Addition of Singlet and Triplet and the Chiral Rhodium-Complex-Catalyzed Addition of (Methoxycarbonyl)phenylcarbene to 1,3-Dimethylallene;The Journal of Organic Chemistry;1996-01-01

2. Self-induced, photochemical, singlet-oxygen oxidation of 4-nitrobenzenesulfenates to 4-nitrobenzenesulfinates;The Journal of Organic Chemistry;1993-07

3. On the regioselectivity of coupling of substituted allyl radicals. Steric versus FMO control;Tetrahedron;1993-04