Structure and Stereochemistry of Rediocide A, A Highly Modified Daphnane from Trigonostemon reidioides Exhibiting Potent Insecticidal Activity-Reference-Cited by-同舟云学术

Structure and Stereochemistry of Rediocide A, A Highly Modified Daphnane from Trigonostemon reidioides Exhibiting Potent Insecticidal Activity

Published:2000-05-01 Issue:20 Volume:122 Page:4998-4999
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Jayasuriya Hiranthi¹,Zink Deborah L.¹,Singh Suresh B.¹,Borris Robert P.¹,Nanakorn Weerachai¹,Beck Hans T.¹,Balick Michael J.¹,Goetz Michael A.¹,Slayton Lyndia¹,Gregory Lynn¹,Zakson-Aiken Michelle¹,Shoop Wesley¹,Singh Sheo B.¹

Affiliation:

1. Merck Research Laboratories, P.O. Box 2000 Rahway, New Jersey, 07065 The Forest Herbarium, Royal Forest Department Bangkok, Thailand 10900 Institute of Economic Botany, The New York Botanical Garden Bronx, New York 10458

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja994074q

Reference9 articles.

1. Detailed accounts of ivermectin chemistry and biological activity can be found inIvermectin and Abamectin; Campbell, W. C., Ed.; Springer-Verlag, New York, 1990, pp 1−344.

2. Alkyl 3,7,11-trimethyl-2,4-dodecadienoates, a new class of potent insect growth regulators with juvenile hormone activity

3. The1H shifts of H-5, H-10, and one of the H2-20 signals experienced an upfield shift of ∼0.1 ppm, and H-11 experienced a downfield shift of 0.1 ppm when the1H NMR spectrum was recorded at 40 mM concentrations.

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