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Literature DB >> 22175379

A synthesis of substituted pyrrolidines via a palladium(2+)-catalyzed cyclization. An unusual approach to a carbapenem.

B M Trost, S F Chen.

Abstract

Entities: Chemical

Year: 1986 PMID： 22175379 DOI： 10.1021/ja00279a071

Source DB: PubMed Journal: J Am Chem Soc ISSN： 0002-7863 Impact factor: 15.419

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2 in total

1. Creation and manipulation of common functional groups en route to a skeletally diverse chemical library.

Authors: Jiayue Cui; Jason Hao; Olesya A Ulanovskaya; Joseph Dundas; Jie Liang; Sergey A Kozmin
Journal: Proc Natl Acad Sci U S A Date: 2011-03-07 Impact factor: 11.205

2. Synthesis of heteroatom-containing pyrrolidine derivatives based on Ti(O-iPr)₄ and EtMgBr-catalyzed carbocyclization of allylpropargyl amines with Et₂Zn.

Authors: Rita N Kadikova; Ilfir R Ramazanov; Azat M Gabdullin; Oleg S Mozgovoj; Usein M Dzhemilev
Journal: RSC Adv Date: 2020-05-07 Impact factor: 4.036

2 in total

A synthesis of substituted pyrrolidines via a palladium(2+)-catalyzed cyclization. An unusual approach to a carbapenem.

1. Creation and manipulation of common functional groups en route to a skeletally diverse chemical library.

2. Synthesis of heteroatom-containing pyrrolidine derivatives based on Ti(O-iPr)4 and EtMgBr-catalyzed carbocyclization of allylpropargyl amines with Et2Zn.

2. Synthesis of heteroatom-containing pyrrolidine derivatives based on Ti(O-iPr)₄ and EtMgBr-catalyzed carbocyclization of allylpropargyl amines with Et₂Zn.