Spiroanthraceneoxazolidine as a synthetic equivalent of methanimine in the reaction with donor–acceptor cyclopropanes. Synthesis of diethyl 5-arylpyrrolidine-3,3-dicarboxylates-Reference-Cited by-同舟云学术

Spiroanthraceneoxazolidine as a synthetic equivalent of methanimine in the reaction with donor–acceptor cyclopropanes. Synthesis of diethyl 5-arylpyrrolidine-3,3-dicarboxylates

Published:2016-08 Issue:33 Volume:57 Page:3731-3734
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Buev Evgeny M.,Moshkin Vladimir S.,Sosnovskikh Vyacheslav Y.

Funder

Russian Science Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference57 articles.

1. Cyclische Aldehydderivate als Alkylierungsreagenzien, 2. Mitt. Aminoalkylderivate von 6-Chlor- und 6-Methylthiopurin und von Uracil

2. Mannich reactions of oxazolidines

3. The functionalisation of electron rich aromatic compounds with 1,3-oxazolidines and 1,3-dimethylimidazolidine

4. Tyrosine Kinase Inhibitors. 14. Structure−Activity Relationships for Methyl- amino-Substituted Derivatives of 4-[(3-Bromophenyl)amino]-6-(methylamino)- pyrido[3,4-d]pyrimidine (PD 158780), a Potent and Specific Inhibitor of the Tyrosine Kinase Activity of Receptors for the EGF Family of Growth Factors

5. A one-pot synthesis of tetrahydroisoquinolin-4-ols via a novel acid-catalyzed rearrangement of 5-aryloxazolidines

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4. Reactivity of spiroanthraceneoxazolidines with cyclopropanes: An approach to the oxindole alkaloid scaffold;Tetrahedron Letters;2018-09

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