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  4. Enol Phosphinates and Phosphonates: Practical Electrophiles for Cross-Coupling Strategies
 
research article

Enol Phosphinates and Phosphonates: Practical Electrophiles for Cross-Coupling Strategies

Steel, Patrick G.
•
Woods, Tom M.
2009
Synthesis: Journal of Synthetic Organic Chemistry

Enol phosphinates and phosphonates can be readily prepared from simple lactams in high yields and are both stable and storable. Both these substrates can be employed successfully in homogeneous Suzuki-Miyaura and Stille cross-couplings protocols. Additionally, the phosphonate group can be immobilised on a phenol-on-polystyrene resin and utilised in a simple diversity linker strategy in which the coupled product is cleaved from the resin under Suzuki-Miyaura cross-coupling conditions.

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Type
research article
DOI
10.1055/s-0029-1217067
Web of Science ID

WOS:000272455100024

Author(s)
Steel, Patrick G.
Woods, Tom M.
Date Issued

2009

Publisher

Georg Thieme Verlag

Published in
Synthesis: Journal of Synthetic Organic Chemistry
Issue

22

Start page

3897

End page

3904

Subjects

lactams

•

arylboronic acids

•

stannanes

•

Suzuki-Miyaura coupling

•

Stille coupling

•

resin-bound enol phosphinate

•

Nitrogen-Containing Heterocycles

•

Heteroaryl Boronic Acids

•

Vinyl Phosphates

•

Aryl

•

Efficient

•

Reagents

•

Lactams

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSYNC  
Available on Infoscience
November 30, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/59560
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