Pd-PEPPSI-IPentCl: A Highly Effective Catalyst for the Selective Cross-Coupling of Secondary Organozinc Reagents

2012 ◽  
Vol 124 (45) ◽  
pp. 11516-11519 ◽  
Author(s):  
Matthew Pompeo ◽  
Robert D. J. Froese ◽  
Niloufar Hadei ◽  
Michael G. Organ
Keyword(s):  
Cross Coupling ◽  
Effective Catalyst ◽  
Highly Effective ◽  
Organozinc Reagents

Pd-PEPPSI-IPentCl: A Highly Effective Catalyst for the Selective Cross-Coupling of Secondary Organozinc Reagents

2012 ◽  
Vol 51 (45) ◽  
pp. 11354-11357 ◽  
Author(s):  
Matthew Pompeo ◽  
Robert D. J. Froese ◽  
Niloufar Hadei ◽  
Michael G. Organ
Keyword(s):  
Cross Coupling ◽  
Effective Catalyst ◽  
Highly Effective ◽  
Organozinc Reagents

ChemInform Abstract: Pd-PEPPSI-IPentCl: A Highly Effective Catalyst for the Selective Cross-Coupling of Secondary Organozinc Reagents.

ChemInform ◽  
2013 ◽  
Vol 44 (12) ◽  
pp. no-no
Author(s):  
Matthew Pompeo ◽  
Robert D. J. Froese ◽  
Niloufar Hadei ◽  
Michael G. Organ
Keyword(s):  
Cross Coupling ◽  
Effective Catalyst ◽  
Highly Effective ◽  
Organozinc Reagents

l-Prolinal Dithioacetal: A Highly Effective Organocatalyst for the Direct Nitro-Michael Addition to Selected Cyclic and Aromatic Ketones

Synthesis ◽  
2019 ◽  
Vol 51 (17) ◽  
pp. 3356-3368
Author(s):  
Piotr Pomarański ◽  
Zbigniew Czarnocki
Keyword(s):  
Michael Addition ◽  
Ring Size ◽  
Cyclic Ketones ◽  
Asymmetric Syntheses ◽  
Aromatic Ketones ◽  
Ring Systems ◽  
Effective Catalyst ◽  
Acetophenone Derivatives ◽  
Highly Effective ◽  
Related Compounds

The synthesis of novel l-prolinal dithioacetal and its application as an organocatalyst for the direct Michael addition of cyclic ketones and acetophenone derivatives to trans-β-nitrostyrene and related compounds is described. The prolinal dithioacetal acts as effective catalyst in the case of cyclic ketones of different ring size, in particular five- and six-membered examples, as well as larger and smaller ring systems. High enantioselectivity and diastereoselectivity is observed for different substrates and trans-β-nitrostyrenes. Also, the first asymmetric syntheses of selected 2-methyl-4-nitro-1,3-diphenylbutan-1-one derivatives by application of the obtained organocatalyst is presented.

Cross β-alkylation of primary alcohols catalysed by DMF-stabilized iridium nanoparticles

2021 ◽  
Author(s):  
Masaki Kobayashi ◽  
Hiroki Yamaguchi ◽  
Takeyuki Suzuki ◽  
Yasushi Obora
Keyword(s):  
Primary Alcohols ◽  
Recycling Process ◽  
Catalyst Recycling ◽  
Simple Method ◽  
Benzyl Alcohols ◽  
Effective Catalyst ◽  
Iridium Nanoparticles ◽  
Highly Effective ◽  
Linear Alcohols ◽  
The Cross

A simple method for the cross β-alkylation of linear alcohols with benzyl alcohols in the presence of DMF-stabilized iridium nanoparticles was developed. Furthermore, a highly effective catalyst-recycling process was also developed.

scholarly journals Enantioselective Radical Addition/Cross‐Coupling of Organozinc Reagents, Alkyl Iodides, and Alkenyl Boron Reagents

2019 ◽  
Vol 58 (40) ◽  
pp. 14245-14249 ◽  
Author(s):  
Matteo Chierchia ◽  
Peilin Xu ◽  
Gabriel J. Lovinger ◽  
James P. Morken
Keyword(s):  
Cross Coupling ◽  
Radical Addition ◽  
Alkyl Iodides ◽  
Organozinc Reagents

Highly Effective Catalyst for the Reaction of Trialkylphosphites with C˭X Electrophiles

2011 ◽  
Vol 186 (4) ◽  
pp. 796-798 ◽  
Author(s):  
Olga O. Kolodiazhna ◽  
Anastasia O. Kolodiazhna ◽  
Oleg I. Kolodiazhnyi
Keyword(s):  
Effective Catalyst ◽  
Highly Effective
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