The Stereochemical Outcome of Electrophilic Addition Reactions on the 5,6-Double Bond in the Spinosyns-Reference-Cited by-同舟云学术

The Stereochemical Outcome of Electrophilic Addition Reactions on the 5,6-Double Bond in the Spinosyns

Published:2001-11-14 Issue:25 Volume:66 Page:8431-8435
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

De Amicis Carl V.,Graupner Paul R.,Erickson Jon A.,Paschal Jonathon W.,Kirst Herbert A.,Creemer Lawrence C.,Fanwick Phillip E.¹

Affiliation:

1. Department of Chemistry, Purdue University, Lafayette, Indiana 47907

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo015830p

Reference27 articles.

1. (b) DeAmicis, C. V.; Dripps, J. E.; Hatton, C. J.; Karr, L. L. InPhytochemicals for Pest Control; Hedin, P. A., Hollingworth, R. M., Maser, E. P., Miyamoto, J., Thompson, D. G., Eds.; ACS Symposium Series 658; American Chemical Society: Washington, DC, 1997; pp 144−154.

2. Conversion of Spinosyn A and Spinosyn D to Their Respective 9- and 17-Pseudoaglycones and Their Aglycones.

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