A Protecting‐Group‐Free Synthesis of (−)‐Salvinorin A-Reference-Cited by-同舟云学术

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A Protecting‐Group‐Free Synthesis of (−)‐Salvinorin A

Published:2021-05-02 Issue:29 Volume:27 Page:7968-7973
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Zimdars Patrick¹,Wang Yuzhou¹,Metz Peter¹^ORCID

Affiliation:

1. Fakultät Chemie und Lebensmittelchemie Organische Chemie I Technische Universität Dresden Bergstraße 66 01069 Dresden Germany

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.202100560

Reference106 articles.

1.

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

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

4.

5. Salvinorin A: A potent naturally occurring nonnitrogenous opioid selective agonist

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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. Sharpless Asymmetric Dihydroxylation: An Impressive Gadget for the Synthesis of Natural Products: A Review;Molecules;2023-03-17

5. Six-membered ring systems: with O and/or S atoms;Progress in Heterocyclic Chemistry;2023

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