Cycloaddition Reactions of a Nitrogen-Substituted Oxyallyl Cation with Cyclopentadiene and Substituted Furans. Reaction Conditions, Diastereoselectivity, Regioselectivity, and Transition State Modeling-Reference-Cited by-同舟云学术

Cycloaddition Reactions of a Nitrogen-Substituted Oxyallyl Cation with Cyclopentadiene and Substituted Furans. Reaction Conditions, Diastereoselectivity, Regioselectivity, and Transition State Modeling

Published:1996-01-01 Issue:4 Volume:61 Page:1478-1486
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Walters Michael A.¹,Arcand Helene R.¹

Affiliation:

1. 6128 Burke Laboratory, Department of Chemistry, Dartmouth College, Hanover, New Hampshire 03755

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo951609z

Reference26 articles.

1. Several reviews have appeared which describe this methodology: (a) Hosomi, A.; Tominga, Y. InComprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon Press: Oxford, 1991; Vol. 5, Chapter 5.1, pp 593−615. (b) Mann, J.Tetrahedron1986,42, 4611−4659. (c) Hoffmann, H. M. R.Angew. Chem., Int. Ed. Engl.1984,23, 1−88. (d) Noyori, R.; Hayakawa, Y.Org. React.1983,29, 163−344. (e) Noyori, R.Acc. Chem. Res.1979,12, 61−66.

2. Ambiphilic reactivity of 1,1-dimethoxyacetone

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