Total Synthesis of (−)-Salvinorin A-Reference-Cited by-同舟云学术

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Total Synthesis of (−)-Salvinorin A

Published:2016-11-04 Issue:50 Volume:22 Page:17983-17986
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Line Nathan J.¹,Burns Aaron C.²,Butler Sean C.³,Casbohm Jerry¹,Forsyth Craig J.¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry; The Ohio State University; 100 W. 18th Ave. Columbus OH 43210 USA

2. Dart NeuroScience LLC; 12278 Scripps Summit Dr. San Diego CA 92131 USA

3. Department of Chemistry and Biochemistry; The University of Texas at Tyler; 3900 University Blvd. Tyler TX 75799 USA

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201604853/fullpdf

Reference43 articles.

1. Salvinorin, a new trans-neoclerodane diterpene from Salvia divinorum(Labiatae)

2. Divinorin A, a psychotropic terpenoid, and divinorin B from the hallucinogenic Mexican mint, Salvia divinorum

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. An Overview of Syntheses of Salvinorin A and its Analogues;ChemCatChem;2024-03-12

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. Asymmetric Syntheses of (+)- and (−)-Collybolide Enable Reevaluation of kappa-Opioid Receptor Agonism;ACS Central Science;2022-07-18

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