Intramolecular Diels−Alder Reactions of Ester-Linked 1,3,8-Nonatrienes-Reference-Cited by-同舟云学术

Intramolecular Diels−Alder Reactions of Ester-Linked 1,3,8-Nonatrienes

Published:2005-06-16 Issue:14 Volume:70 Page:5561-5570
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cayzer Tory N.¹,Paddon-Row Michael N.¹,Moran Damian¹,Payne Alan D.¹,Sherburn Michael S.¹,Turner Peter¹

Affiliation:

1. Research School of Chemistry, Australian National University, Canberra, ACT 0200, Australia, School of Chemistry, The University of New South Wales, Sydney, NSW 2052, Australia, and School of Chemistry, University of Sydney, Sydney, NSW 2006, Australia

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0505829

Reference53 articles.

1. Origins of Stereoselectivity in Intramolecular Diels−Alder Cycloadditions of Dienes and Dienophiles Linked by Ester and Amide Tethers

2. Experimental Determination of the Activation Parameters and Stereoselectivities of the Intramolecular Diels−Alder Reactions of 1,3,8-Nonatriene, 1,3,9-Decatriene, and 1,3,10-Undecatriene and Transition State Modeling with the Monte Carlo-Jumping Between Wells/Molecular Dynamics Method

3. Effect of multiple halide substituents on the acidity of methanes and methyl radicals. Electron affinities of chloro- and fluoromethyl radicals

4. Empirical force field models for the transition states of intramolecular Diels-Alder reactions based upon ab initio transition structures

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