A new, simple, and mild azidolysis of vinylepoxides-Reference-Cited by-同舟云学术

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A new, simple, and mild azidolysis of vinylepoxides

Published:2011-07 Issue:30 Volume:52 Page:3895-3896
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Righi Giuliana,Manni Livia Salvati,Bovicelli Paolo,Pelagalli Romina

Funder

Ministero dell’Istruzione, dell’Università e della Ricerca

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Formal total synthesis of (−)-balanol: a potent PKC inhibitor

2. Total Synthesis of Hyacinthacine A1, a Glycosidase Inhibitor

3. Synthesis of (−)-(4R,5R)-muricatacin using a regio- and stereospecific ring-opening of a vinyl epoxide

4. Enantioselective Synthesis of (−)-LL-C10037α from Benzoquinone

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2. Total stereocontrolled synthesis of a novel pyrrolizidine iminosugar;Carbohydrate Research;2022-01

3. Ring Opening Reactions of Epoxides. A Review;Organic Preparations and Procedures International;2021-11-08

4. Montmorillonite K10 catalyzed highly regioselective azidolysis of epoxides: A short and efficient synthesis of phenylglycine;Synthetic Communications;2018-11-15

5. Asymmetric routes toward polyhydroxylated pyrrolidines: Synthesis of 1,4-dideoxy-1,4-imino-d-galactitol and 1,4-dideoxy-1,4-imino-d-glucitol;Carbohydrate Research;2016-11

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