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  4. Pd(0)-Catalyzed Oxy- and Aminoalkynylation of Olefins for the Synthesis of Tetrahydrofurans and Pyrrolidines
 
research article

Pd(0)-Catalyzed Oxy- and Aminoalkynylation of Olefins for the Synthesis of Tetrahydrofurans and Pyrrolidines

Nicolai, Stefano  
•
Waser, Jerome  
2011
Organic Letters

The first Pd(0)-catalyzed intramolecular oxy- and aminoalkynylation of nonactivated olefins is reported. The reaction gives access to important tetrahydrofuran and pyrrolidine heterocycles with high diastereoselectivity. The unique synthetic potential of acetylenes is further exploited to access key building blocks for the synthesis of bioactive natural products.

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Type
research article
DOI
10.1021/ol2029383
Web of Science ID

WOS:000297274700048

Author(s)
Nicolai, Stefano  
Waser, Jerome  
Date Issued

2011

Publisher

American Chemical Society

Published in
Organic Letters
Volume

13

Start page

6324

End page

6327

Subjects

Palladium-Catalyzed Synthesis

•

C-H Bonds

•

Stereoselective-Synthesis

•

Terminal Alkynes

•

Carboamination Reactions

•

Aminoalkynylation

•

Organic Synthesis

•

Heterocycles

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSO  
Available on Infoscience
December 16, 2011
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/73215
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