Construction of Enantiomerically Enriched Diazo Compounds Using Diazo Esters as Nucleophiles: Chiral Lewis Base Catalysis

2013 ◽  
Vol 125 (24) ◽  
pp. 6408-6412 ◽  
Author(s):  
Haibin Mao ◽  
Aijun Lin ◽  
Yan Shi ◽  
Zhijie Mao ◽  
Xuebin Zhu ◽  
...  
Keyword(s):  
Lewis Base ◽  
Base Catalysis ◽  
Diazo Compounds ◽  
Diazo Esters

Construction of Enantiomerically Enriched Diazo Compounds Using Diazo Esters as Nucleophiles: Chiral Lewis Base Catalysis

2013 ◽  
Vol 52 (24) ◽  
pp. 6288-6292 ◽  
Author(s):  
Haibin Mao ◽  
Aijun Lin ◽  
Yan Shi ◽  
Zhijie Mao ◽  
Xuebin Zhu ◽  
...  
Keyword(s):  
Lewis Base ◽  
Base Catalysis ◽  
Diazo Compounds ◽  
Diazo Esters

ChemInform Abstract: Construction of Enantiomerically Enriched Diazo Compounds Using Diazo Esters as Nucleophiles: Chiral Lewis Base Catalysis.

ChemInform ◽  
2013 ◽  
Vol 44 (44) ◽  
pp. no-no
Author(s):  
Haibin Mao ◽  
Aijun Lin ◽  
Yan Shi ◽  
Zhijie Mao ◽  
Xuebin Zhu ◽  
...  
Keyword(s):  
Lewis Base ◽  
Base Catalysis ◽  
Diazo Compounds ◽  
Diazo Esters

scholarly journals Dual metal and Lewis base catalysis approach for asymmetric synthesis of dihydroquinolines and the α-arylation of aldehydes via N-acyliminium ions

2015 ◽  
Vol 51 (87) ◽  
pp. 15788-15791 ◽  
Author(s):  
Chandra M. R. Volla ◽  
Eleonora Fava ◽  
Iuliana Atodiresei ◽  
Magnus Rueping
Keyword(s):  
Asymmetric Synthesis ◽  
Catalytic System ◽  
Optically Active ◽  
Lewis Base ◽  
Base Catalysis ◽  
Asymmetric Addition ◽  
Acyliminium Ions ◽  
Indium Triflate ◽  
Dual Metal

A dual catalytic system consisting of indium triflate and a chiral imidazolidinone catalyzes the asymmetric addition of aldehydes to N-acyl quinoliniums furnishing optically active dihydroquinolines in good yields and excellent selectivities.

Lewis base mediated halogenation/semipinacol rearrangement of diazo compounds: new access to α-halo-quaternary ketones

2014 ◽  
Vol 50 (68) ◽  
pp. 9773-9775 ◽  
Author(s):  
Haibin Mao ◽  
Zhongkai Tang ◽  
Hongwen Hu ◽  
Yixiang Cheng ◽  
Wen-Hua Zheng ◽  
...  
Keyword(s):  
Lewis Base ◽  
Diazo Compounds ◽  
Semipinacol Rearrangement

A novel halogenation/semipinacol rearrangement of α-diazo alcohol catalyzed by Lewis base has been developed through a carbene-free mechanism.

ChemInform Abstract: A New Motif for Lewis Base Catalysis: Asymmetric Reduction of β-Enamino Esters

ChemInform ◽  
2012 ◽  
Vol 43 (11) ◽  
pp. no-no
Author(s):  
Andreas Weickgennat ◽  
Martin Oestreich
Keyword(s):  
Asymmetric Reduction ◽  
Lewis Base ◽  
Base Catalysis

ChemInform Abstract: Lewis Base Assisted Broensted Base Catalysis: Direct Regioselective Asymmetric Vinylogous Alkylation of Allylic Sulfones.

ChemInform ◽  
2011 ◽  
Vol 42 (52) ◽  
pp. no-no
Author(s):  
Lin Jiang ◽  
Qian Lei ◽  
Xin Huang ◽  
Hai-Lei Cui ◽  
Xue Zhou ◽  
...  
Keyword(s):  
Lewis Base ◽  
Base Catalysis
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