A facile synthesis of 3-allyl-4-hydrazinocyclopentenes by the palladium/Lewis acid mediated ring opening of bicyclic hydrazines with allyltributyltin and allyltrimethylsilane-Reference-Cited by-同舟云学术

A facile synthesis of 3-allyl-4-hydrazinocyclopentenes by the palladium/Lewis acid mediated ring opening of bicyclic hydrazines with allyltributyltin and allyltrimethylsilane

Published:2006-04 Issue:17 Volume:62 Page:3997-4002
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Sajisha V.S.,Smitha Mohanlal,Anas S.,Radhakrishnan K.V.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference45 articles.

1. New developments in the enantioselective synthesis of cyclopentyl carbocyclic nucleosides

2. Synthesis and Biological Activity of Natural Aminocyclopentitol Glycosidase Inhibitors: Mannostatins, Trehazolin, Allosamidins, and Their Analogues

3. Synthesis of a potent aminocyclitol α-mannosidase inhibitor, 1 l -(1,2,3,5/4)-5-amino-4- O -methyl-1,2,3,4-cyclopentanetetrol

4. A direct, stereocontrolled total synthesis of the 9,11-azo analog of the prostaglandin endoperoxide, PGH2

5. Enantioselective syntheses of carbocyclic ribavirin and its analogs: linear versus convergent approaches

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