Remote Substituent Effects in Ruthenium-Catalyzed [2+2] Cycloadditions: An Experimental and Theoretical Study-Reference-Cited by-同舟云学术

Remote Substituent Effects in Ruthenium-Catalyzed [2+2] Cycloadditions: An Experimental and Theoretical Study

Published:2006-04-07 Issue:10 Volume:71 Page:3793-3803
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Peng¹,Jordan Robert W.¹,Kibbee Steven P.¹,Goddard John D.¹,Tam William¹

Affiliation:

1. Guelph-Waterloo Centre for Graduate Work in Chemistry and Biochemistry, Department of Chemistry, University of Guelph, Guelph, Ontario, Canada N1G 2W1

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo060103l

Reference63 articles.

1. Inductive and Resonance Effects of Substituents on π-Face Selection

2. Diastereofacial selection in nucleophilic additions to unsymmetrically substituted trigonal carbons

3. Regioselectivity of electrophilic additions to 7-oxabicyclo[2.2.1]heptenes controlled by remote substituents. Arenesulfonyl substituted 7-oxabicyclo[2.2.1]heptenes as stereo- and regioselective chiral dienophiles

4. Regioselective electrophilic additions to 2-oxygenated-7-oxabicyclo[2.2.1]Hept-5-enes: A simple entry into the 4,7-dioxatricyclo[3.2.1.03,6]octaneskeleton

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