Asymmetric Synthesis of Salvinorin A, A Potent κ Opioid Receptor Agonist-Reference-Cited by-同舟云学术

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Asymmetric Synthesis of Salvinorin A, A Potent κ Opioid Receptor Agonist

Published:2007-06-30 Issue:29 Volume:129 Page:8968-8969
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Scheerer Jonathan R.¹,Lawrence Jonathan F.¹,Wang Grace C.¹,Evans David A.¹

Affiliation:

1. Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja073590a

Reference27 articles.

1. Neo-clerodane Diterpenes from the Hallucinogenic Sage Salvia divinorum

2. Synthesis and in vitro evaluation of salvinorin A analogues: Effect of configuration at C(2) and substitution at C(18)

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2. Formal Synthesis of (±)‐Salvinorin A via Gold(I) Catalysis;Chemistry – A European Journal;2023-07-26

3. A Route to Potent, Selective, and Biased Salvinorin Chemical Space;ACS Central Science;2023-07-12

4. Enantioselective and collective total synthesis of pentacyclic 19-nor-clerodanes;Chemical Science;2023

5. Formal Total Synthesis of Salvinorin A;ChemistryOpen;2022-02-26

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