First Stereoselective Total Synthesis and Biological Evaluation of Amphidinin B and Its Analogues-Reference-Cited by-同舟云学术

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First Stereoselective Total Synthesis and Biological Evaluation of Amphidinin B and Its Analogues

Published:2010-12-14 Issue:4 Volume:2011 Page:696-706
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Yadav Jhillu S.,Reddy A. Srinivas,Reddy Ch. Suresh,Reddy Basi V. Subba,Saddanapu Venkateshwarlu,Addlagatta Anthony

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference41 articles.

1. Amphidinolides: Unique Macrolides from Marine Dinoflagellates

2. Chemistry of Potent Anti-Cancer Compounds, Amphidinolides

3. Bioactive Macrolides and Polyketides from Marine Dinoflagellates of the Genus Amphidinium

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1. Synthesis of chiral propargyl alcohols following the base-induced elimination protocol: application in the total synthesis of natural products;New Journal of Chemistry;2020

2. Synthesis of Δ20-Ginsenosides Rh4, (20E)-Rh3, Rg6, and Rk1: A General Approach To Access Dehydrated Ginsenosides;The Journal of Organic Chemistry;2018-02-20

3. Total synthesis of amphidinins E, F and epi-amphidinin F;Organic Chemistry Frontiers;2018

4. Synthesis of β-(2,2-diethoxyethyl)-substituted (allyl)tributylstannane and its application to asymmetric allylation;Russian Journal of Organic Chemistry;2016-02

5. Applications of oxazolidinones as chiral auxiliaries in the asymmetric alkylation reaction applied to total synthesis;RSC Advances;2016

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