Titanium(IV)-Promoted Regioselective Nucleophilic Ring-Opening Reaction of Chiral Epoxyallyl Alcohols with Acids as a Tool for Ready Access to Chiral 1,2,3-Triol Monoesters: Application to Stereoselective Total Synthesis of Macrolides-Reference-Cited by-同舟云学术

Titanium(IV)-Promoted Regioselective Nucleophilic Ring-Opening Reaction of Chiral Epoxyallyl Alcohols with Acids as a Tool for Ready Access to Chiral 1,2,3-Triol Monoesters: Application to Stereoselective Total Synthesis of Macrolides

Published:2011-12-20 Issue:1 Volume:77 Page:674-679
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Radha Krishna Palakodety¹,Ramana D. Venkata¹

Affiliation:

1. D-211, Discovery Laboratory, Organic & Biomolecular Chemistry Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500607, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo202199g

Reference39 articles.

1. Enantiospecific Semisynthesis of (+)-Almuheptolide-A, a Novel Natural Heptolide Inhibitor of the Mammalian Mitochondrial Respiratory Chain

2. Pinolidoxin, a phytotoxic nonenolide from Ascochyta pinodes

3. Herbicidal Potential of Stagonolide, a New Phytotoxic Nonenolide from Stagonospora cirsii

4. Conformational Behavior and Absolute Stereostructure of Two Phytotoxic Nonenolides from the Fungus Phoma herbarum

5. Stagonolides B−F, Nonenolides Produced by Stagonospora cirsii, a Potential Mycoherbicide of Cirsium arvense

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