Total Syntheses of Clerodane Diterpenoids—A Review-Reference-Cited by-同舟云学术

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Total Syntheses of Clerodane Diterpenoids—A Review

Published:2019-06 Issue:6 Volume:14 Page:1934578X1984361
ISSN:1934-578X
Container-title:Natural Product Communications
language:en
Short-container-title:Natural Product Communications

Author:

Hagiwara Hisahiro¹

Affiliation:

1. Graduate School of Science and Technology, Niigata University, Nishiku, Niigata, Japan

Abstract

Total syntheses of clerodane diterpenoids have been reviewed from the literature since 2000.

Publisher

SAGE Publications

Subject

Complementary and alternative medicine,Plant Science,Drug Discovery,Pharmacology,General Medicine

Link

http://journals.sagepub.com/doi/pdf/10.1177/1934578X19843613

Reference54 articles.

1. Clerodane diterpenes: sources, structures, and biological activities

2. Absolute stereochemistries of 3-epicaryoptin, caryoptin, and clerodin as determined by chiroptical methods

3. The ent-neo-clerodane absolute configuration of ajugarins

4. X-Ray crystal structure of 12-bromoajugarin-I and conclusion on the absolute configuration of ajugarins

5. The crystal structure of 3-epicaryoptin and the reversal of the currently accepted absolute configuration of clerodin

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1. Structural Revision of Tinotufolins from Tinospora crispa Leaves Guided by Empirical Rules and DFT Calculations;Journal of Natural Products;2024-02-15

2. Anti-Inflammatory and Cytotoxic Activities of Clerodane-Type Diterpenes;Molecules;2023-06-13

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

4. SmI ₂ ‐mediated C‐alkylation of Ketones with Alcohols under Microwave Conditions: A Novel Route to Alkylated Ketones;Chemistry – An Asian Journal;2022-03-09

5. New clerodane diterpenoids from Solidago altissima and stereochemical elucidation via 13C NMR chemical shift analysis;Tetrahedron;2022-03

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