Selective Reduction and Dehydrogenation of 6-Benzylideneoctahydropyrrolo[1,2-a]Pyrimidines and 5-Benzylidenehexahydropyrrolo[1,2-a]Imidazoles as New Approaches to N-(ω-Aminoalkyl)Pyrrolidines and Bicyclic Amidines-Reference-Cited by-同舟云学术

Selective Reduction and Dehydrogenation of 6-Benzylideneoctahydropyrrolo[1,2-a]Pyrimidines and 5-Benzylidenehexahydropyrrolo[1,2-a]Imidazoles as New Approaches to N-(ω-Aminoalkyl)Pyrrolidines and Bicyclic Amidines

Published:2013-01 Issue:1 Volume:23 Page:31-33
ISSN:0959-9436
Container-title:Mendeleev Communications
language:en
Short-container-title:Mendeleev Communications

Author:

Shavrin Konstantin N.,Gvozdev Valentin D.,Nefedov Oleg M.

Publisher

Elsevier BV

Subject

General Chemistry

Reference29 articles.

1. Asymmetric Synthesis of cis- and trans-2,5-Disubstituted Pyrrolidines from 3-Oxo Pyrrolidine 2-Phosphonates: Synthesis of (+)-Preussin and Analogs

2. An Efficient Synthesis of 5-(or 6-)Arylbenzoindolizidine and -quinolizidine Derivatives

3. A new route to ene carbamates, precursors to benzoindolizinones through sequential asymmetric hydrogenation and cyclization

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