Organocatalytic Asymmetric Aldol Reaction of Hydroxyacetone with β,γ-Unsaturated α-Keto Esters: Facile Access to Chiral Tertiary Alcohols

Organic Letters ◽

10.1021/ol2021274 ◽

2011 ◽

Vol 13 (19) ◽

pp. 5248-5251 ◽

Author(s):

Chen Liu ◽

Xiaowei Dou ◽

Yixin Lu

Keyword(s):

Aldol Reaction ◽

Asymmetric Aldol ◽

Tertiary Alcohols ◽

Keto Esters ◽

Asymmetric Aldol Reaction ◽

Chiral Tertiary Alcohols

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ChemInform Abstract: Organocatalytic Asymmetric Aldol Reaction of Hydroxyacetone with β,γ-Unsaturated α-Keto Esters: Facile Access to Chiral Tertiary Alcohols.

10.1002/chin.201206056 ◽

2012 ◽

Vol 43 (6) ◽

pp. no-no

Author(s):

Chen Liu ◽

Xiaowei Dou ◽

Yixin Lu

Keyword(s):

Aldol Reaction ◽

Asymmetric Aldol ◽

Tertiary Alcohols ◽

Keto Esters ◽

Asymmetric Aldol Reaction ◽

Chiral Tertiary Alcohols

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ChemInform Abstract: Asymmetric Aldol Reaction of α-Keto Esters with Isocyanoacetate and Isocyanoacetamide Catalyzed by a Chiral Ferrocenylphosphine/Gold(I) Complex.

10.1002/chin.199014166 ◽

1990 ◽

Vol 21 (14) ◽

Author(s):

Y. ITO ◽

M. SAWAMURA ◽

H. HAMASHIMA ◽

T. EMURA ◽

T. HAYASHI

Keyword(s):

Aldol Reaction ◽

Asymmetric Aldol ◽

Keto Esters ◽

Asymmetric Aldol Reaction

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A General Asymmetric Aldol Reaction of Silyl Ketene Acetals Derived from Simple Esters to Aryl Î±-Keto Esters

European Journal of Organic Chemistry ◽

10.1002/ejoc.200901086 ◽

2009 ◽

Vol 2009 (35) ◽

pp. 6109-6111 ◽

Author(s):

Julie Le Engers ◽

Brian L. Pagenkopf

Keyword(s):

Aldol Reaction ◽

Asymmetric Aldol ◽

Keto Esters ◽

Asymmetric Aldol Reaction ◽

Ketene Acetals ◽

Silyl Ketene Acetals

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ChemInform Abstract: A General Asymmetric Aldol Reaction of Silyl Ketene Acetals Derived from Simple Esters to Aryl α-Keto Esters.

10.1002/chin.201015075 ◽

2010 ◽

Vol 41 (15) ◽

Author(s):

Julie Le Engers ◽

Brian L. Pagenkopf

Keyword(s):

Aldol Reaction ◽

Asymmetric Aldol ◽

Keto Esters ◽

Asymmetric Aldol Reaction ◽

Ketene Acetals ◽

Silyl Ketene Acetals

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Organocatalytic Asymmetric Aldol Reaction of Ketones with β,γ-Unsaturated α-Keto Esters: An Efficient Access to Chiral Tertiary Alcohol Skeletons

Advanced Synthesis & Catalysis ◽

10.1002/adsc.201000982 ◽

2011 ◽

Vol 353 (7) ◽

pp. 1179-1184 ◽

Author(s):

Pengfei Li ◽

Sau Hing Chan ◽

Albert S. C. Chan ◽

Fuk Yee Kwong

Keyword(s):

Aldol Reaction ◽

Tertiary Alcohol ◽

Asymmetric Aldol ◽

Keto Esters ◽

Efficient Access ◽

Asymmetric Aldol Reaction

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Direct catalytic asymmetric aldol reaction of β-keto esters with formaldehyde promoted by a dinuclear Ni2-Schiff base complex

Chemical Communications ◽

10.1039/b912380f ◽

2009 ◽

pp. 5138 ◽

Author(s):

Shinsuke Mouri ◽

Zhihua Chen ◽

Shigeki Matsunaga ◽

Masakatsu Shibasaki

Keyword(s):

Schiff Base ◽

Aldol Reaction ◽

Schiff Base Complex ◽

Asymmetric Aldol ◽

Base Complex ◽

Keto Esters ◽

Asymmetric Aldol Reaction ◽

Catalytic Asymmetric

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ChemInform Abstract: Organocatalytic Asymmetric Aldol Reaction of Ketones with β,γ-Unsaturated α-Keto Esters: An Efficient Access to Chiral Tertiary Alcohol Skeletons.

10.1002/chin.201138030 ◽

2011 ◽

Vol 42 (38) ◽

pp. no-no

Author(s):

Pengfei Li ◽

Sau Hing Chan ◽

Albert S. C. Chan ◽

Fuk Yee Kwong

Keyword(s):

Aldol Reaction ◽

Tertiary Alcohol ◽

Asymmetric Aldol ◽

Keto Esters ◽

Efficient Access ◽

Asymmetric Aldol Reaction

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ChemInform Abstract: Direct Catalytic Asymmetric Aldol Reaction of Î²-Keto Esters with Formaldehyde Promoted by a Dinuclear Ni2-Schiff Base Complex.

10.1002/chin.201001025 ◽

2010 ◽

Vol 41 (1) ◽

pp. no-no

Author(s):

Shinsuke Mouri ◽

Zhihua Chen ◽

Shigeki Matsunaga ◽

Masakatsu Shibasaki

Keyword(s):

Schiff Base ◽

Aldol Reaction ◽

Schiff Base Complex ◽

Asymmetric Aldol ◽

Base Complex ◽

Keto Esters ◽

Asymmetric Aldol Reaction ◽

Catalytic Asymmetric

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Dual Proline/Water Compatible Lewis Acid Activation: a Biomimetic Approach for Direct Asymmetric Aldol Reaction

10.3390/ecsoc-13-00193 ◽

2009 ◽

Author(s):

Maël Penhoat ◽

Christian Rolando ◽

Didier Barbry

Keyword(s):

Aldol Reaction ◽

Acid Activation ◽

Asymmetric Aldol ◽

Asymmetric Aldol Reaction ◽

Biomimetic Approach

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Faculty Opinions recommendation of Development of highly diastereo- and enantioselective direct asymmetric aldol reaction of a glycinate Schiff base with aldehydes catalyzed by chiral quaternary ammonium salts.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1020518.232638 ◽

2004 ◽

Author(s):

Carlos F Barbas

Keyword(s):

Schiff Base ◽

Quaternary Ammonium ◽

Aldol Reaction ◽

Quaternary Ammonium Salts ◽

Ammonium Salts ◽

Asymmetric Aldol ◽

Asymmetric Aldol Reaction

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