1,3-Dimethoxy-5-methylene-1,3-cyclohexadiene Compounds with Leaving Groups at C6: Generation, Solvolytic Reactivity, and Their Importance in the Photochemistry of 3,5-Dimethoxybenzyl Derivatives-Reference-Cited by-同舟云学术

1,3-Dimethoxy-5-methylene-1,3-cyclohexadiene Compounds with Leaving Groups at C6: Generation, Solvolytic Reactivity, and Their Importance in the Photochemistry of 3,5-Dimethoxybenzyl Derivatives

Published:2000-07-01 Issue:15 Volume:65 Page:4698-4705
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

DeCosta D. P.¹,Howell N.¹,Pincock A. L.¹,Pincock J. A.¹,Rifai S.¹

Affiliation:

1. Department of Chemistry, Dalhousie University Halifax, Nova Scotia, Canada, B3H 4J3, and Department of Chemistry, Colombo University, Colombo, Sri Lanka

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo000387o

Reference52 articles.

1. The Role of Nonaromatic Isomers in the Photochemistry of 3,5-Dimethoxybenzyl Acetate

2. Fleming, S. A.; Pincock, J. A.Organic Molecular Photochemistry; M. Dekker: New York, 1999; Vol. 3, pp 211−281.

3. Photochemistry of Arylmethyl Esters in Nucleophilic Solvents: Radical Pair and Ion Pair Intermediates

4. Rates of decarboxylation of acyloxy radicals formed in the photocleavage of substituted 1-naphthylmethyl alkanoates

5. Direct Observation of Carbon−Carbon Bond Cleavage in Ultrafast Decarboxylations

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