Oxidative addition of N-aminophthalimide to thiophene and selenophene: the first example of a 5-thia(seleno)-3,7-diazatricyclo[4.1.0.02,4]heptane system-Reference-Cited by-同舟云学术

Oxidative addition of N-aminophthalimide to thiophene and selenophene: the first example of a 5-thia(seleno)-3,7-diazatricyclo[4.1.0.02,4]heptane system

Published:2011-08 Issue:31 Volume:52 Page:4048-4050
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Pankova Alena S.,Blandov Alexander N.,Bulanova Maria K.,Selivanov Stanislav I.,Ananyev Ivan V.,Kuznetsov Mikhail A.

Funder

Saint Petersburg State University

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

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2. Diastereoselective Control Through Hydrogen Bonding in the Aziridination of the Chiral Allylic Alcohols by Acetoxyaminoquinazolinone

3. Au(I)-Catalyzed Rearrangement Reaction of Propargylic Aziridine: Synthesis of Trisubstituted and Cycloalkene-Fused Pyrroles

4. On the scope of diastereoselective aziridination of various chiral auxiliaries derived N- and O-enones with N-aminophthalimide in the presence of lead tetraacetate

5. Lewis Acid Catalyzed [1,3]-Sigmatropic Rearrangement of Vinyl Aziridines

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