scholarly journals Highly Diastereoselective 1,2-Asymmetric Addition of Dialkylzincs to Chiral 2-Phenylpropanal Catalyzed by Amino Alcohol

1990 ◽  
Vol 63 (7) ◽  
pp. 2129-2130 ◽  
Author(s):  
Kenso Soai ◽  
Seiji Niwa ◽  
Toshihiro Hatanaka
Keyword(s):  
Amino Alcohol ◽  
Asymmetric Addition

A new pyrrolidine-derived atropisomeric amino alcohol as a highly efficient chiral ligand for the asymmetric addition of diethylzinc to aldehydes

2014 ◽  
Vol 55 (50) ◽  
pp. 6891-6894 ◽  
Author(s):  
Ferenc Faigl ◽  
Zsuzsa Erdélyi ◽  
Szilvia Deák ◽  
Miklós Nyerges ◽  
Béla Mátravölgyi
Keyword(s):  
Amino Alcohol ◽  
Chiral Ligand ◽  
Asymmetric Addition ◽  
Highly Efficient

Polystyrene-Supported Amino Alcohol Ligands for the Heterogeneous Asymmetric Addition of Phenyl Zinc Reagents to Aldehydes.

ChemInform ◽  
2006 ◽  
Vol 37 (15) ◽  
Author(s):  
David Castellnou ◽  
Montserrat Fontes ◽  
Ciril Jimeno ◽  
Daniel Font ◽  
Lluis Sola ◽  
...  
Keyword(s):  
Amino Alcohol ◽  
Asymmetric Addition

ChemInform Abstract: A New Pyrrolidine-Derived Atropisomeric Amino Alcohol as a Highly Efficient Chiral Ligand for the Asymmetric Addition of Diethylzinc to Aldehydes.

ChemInform ◽  
2015 ◽  
Vol 46 (18) ◽  
pp. no-no
Author(s):  
Ferenc Faigl ◽  
Zsuzsa Erdelyi ◽  
Szilvia Deak ◽  
Miklos Nyerges ◽  
Bela Matravoelgyi
Keyword(s):  
Amino Alcohol ◽  
Chiral Ligand ◽  
Asymmetric Addition ◽  
Highly Efficient

Novel Polymer-Bound Amino Alcohol Ligands for the Asymmetric Addition of Diethylzinc to Aldehydes.

ChemInform ◽  
2007 ◽  
Vol 38 (45) ◽  
Author(s):  
Philip C. Bulman Page ◽  
Steven M. Allin ◽  
Suzanne J. Dilly ◽  
Benjamin R. Buckley
Keyword(s):  
Amino Alcohol ◽  
Asymmetric Addition

Enantioselective Addition of Alkynyl Esters and Ethers to Aldehydes Catalyzed by a Cyclopropyl Amino Alcohol Based Zinc Catalyst

Synlett ◽  
2019 ◽  
Vol 31 (01) ◽  
pp. 60-64
Author(s):  
Yun Zhou ◽  
Lifeng Wang ◽  
Shuoning Li ◽  
Sijie Ma ◽  
Patrick J. Walsh ◽  
...  
Keyword(s):  
Functional Groups ◽  
Amino Alcohol ◽  
Carbon Chain ◽  
Enantioselective Synthesis ◽  
Asymmetric Addition ◽  
Enantioselective Addition

A novel and highly enantioselective synthesis of hydroxyalkynyl esters and ethers through the asymmetric addition of alkynyl esters or ethers to aldehydes promoted by a cyclopropyl amino alcohol based zinc catalyst has been developed. The method afforded a library of new enantioenriched hydroxyalkynol esters and ethers (up to 93% yield; 95% ee), and it was compatible with a broad range of functional groups. Moreover, it could be used in the synthesis of carbon-chain-elongated enantioenriched hydroxyalkynol esters and (2R,5R)-musclide-A1, a cardiotonic potentiating principle from musk.

Asymmetric addition of diethylzinc to aldehydes catalyzed by a camphor-derived β-amino alcohol

2009 ◽  
Vol 20 (13) ◽  
pp. 1556-1560 ◽  
Author(s):  
Zhi-Long Wu ◽  
Hsyueh-Liang Wu ◽  
Ping-Yu Wu ◽  
Biing-Jiun Uang
Keyword(s):  
Amino Alcohol ◽  
Asymmetric Addition
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