Suzuki-Miyaura cross-coupling catalyzed by protein-stabilized palladium nanoparticles under aerobic conditions in water: application to a one-pot chemoenzymatic enantioselective synthesis of chiral biaryl alcohols-Reference-Cited by-同舟云学术

Suzuki-Miyaura cross-coupling catalyzed by protein-stabilized palladium nanoparticles under aerobic conditions in water: application to a one-pot chemoenzymatic enantioselective synthesis of chiral biaryl alcohols

Published:2009 Issue:12 Volume:11 Page:1929
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Prastaro A.,Ceci P.,Chiancone E.,Boffi A.,Cirilli R.,Colone M.,Fabrizi G.,Stringaro A.,Cacchi S.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2009/GC/B915184B

Reference30 articles.

1. Organic Reactions in Aqueous Media with a Focus on Carbon−Carbon Bond Formations: A Decade Update

2. Copper-free Sonogashira coupling reaction catalyzed by MCM-41-supported thioether palladium(0) complex in water under aerobic conditions

3. Convenient Synthesis of New Anionic Water-Soluble Phosphanes and Applications in Inter- and Intramolecular Heck Reactions

4. Controlled mono and double Heck reactions in water catalyzed by an oxime-derived palladacycle

5. Synthesis of methylated resveratrol and analogues by Heck reactions in organic and aqueous solvents

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