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  4. Organocatalytic Enantioselective One-Pot Four-Component Ugi-Type Multicomponent Reaction for the Synthesis of Epoxy-tetrahydropyrrolo[3,4-
 
research article

Organocatalytic Enantioselective One-Pot Four-Component Ugi-Type Multicomponent Reaction for the Synthesis of Epoxy-tetrahydropyrrolo[3,4-

Su, Yingpeng
•
Bouma, Marinus J.
•
Alcaraz, Lilian
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2012
Chemistry - A European Journal

In the presence of a catalytic amount of chiral BINOL-derived phosphoric acid (TRIP), reaction of an α-isocyanoacetate 1, an aldehyde 2, an aniline 3 followed by addition of a toluene solution of α,β-unsaturated acyl chloride 5 afforded oxa-bridged tricycle 6 in excellent yield, diastereoselectivity and enantioselectivity. Six chemical bonds, five stereogenic centers, three cycles were formed in this one pot four-component reaction.

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Type
research article
DOI
10.1002/chem.201202174
Web of Science ID

WOS:000309238400010

Author(s)
Su, Yingpeng
Bouma, Marinus J.
Alcaraz, Lilian
Stocks, Mike
Furber, Mark
Masson, Géraldine
Zhu, Jieping  
Date Issued

2012

Publisher

Wiley-Blackwell

Published in
Chemistry - A European Journal
Volume

18

Issue

40

Start page

12624

End page

12627

Subjects

multicomponent reactions

•

Brønsted acid

•

organocatalysis

•

Ugi Reaction

•

α-isocyanoacetate

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSPN  
Available on Infoscience
October 1, 2012
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/85832
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