Structure–Reactivity Relationships in Lithiated Evans Enolates: Influence of Aggregation and Solvation on the Stereochemistry and Mechanism of Aldol Additions

Evan H. Tallmadge; Janis Jermaks; David B. Collum

doi:10.1021/jacs.5b10980

Structure–Reactivity Relationships in Lithiated Evans Enolates: Influence of Aggregation and Solvation on the Stereochemistry and Mechanism of Aldol Additions

Journal of the American Chemical Society ◽

10.1021/jacs.5b10980 ◽

2015 ◽

Vol 138 (1) ◽

pp. 345-355 ◽

Cited By ~ 16

Author(s):

Evan H. Tallmadge ◽

Janis Jermaks ◽

David B. Collum

Keyword(s):

Aldol Additions

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The Effects of a Remote Stereogenic Center in the Lewis Base Catalyzed Aldol Additions of Chiral Trichlorosilyl Enolates.

ChemInform ◽

10.1002/chin.200311081 ◽

2003 ◽

Vol 34 (11) ◽

Author(s):

Scott E. Denmark ◽

Shinji Fujimori

Keyword(s):

Lewis Base ◽

Aldol Additions ◽

Stereogenic Center

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Computational study of the syn,anti-selective aldol additions of lithiated bis-lactim ether to 1,3-dioxolane-4-carboxaldehydes

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(02)00479-2 ◽

2002 ◽

Vol 13 (17) ◽

pp. 1863-1873 ◽

Cited By ~ 7

Author(s):

Marı́a Ruiz ◽

Vicente Ojea ◽

José M Quintela

Keyword(s):

Computational Study ◽

Aldol Additions ◽

Lactim Ether

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ChemInform Abstract: Chelation Controlled Aldol Additions of the Enolsilane Derived from tert.-Butyl Thioacetate: A Stereoselective Approach to 1β-Methylthienamycin.

ChemInform ◽

10.1002/chin.198904316 ◽

1989 ◽

Vol 20 (4) ◽

Author(s):

C. GENNARI ◽

P. G. COZZI

Keyword(s):

Tert Butyl ◽

Aldol Additions

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Three-Center Diastereoselective Aldol Additions ofβ-Lactone Enolates to Aldehydes

Angewandte Chemie International Edition in English ◽

10.1002/anie.198207771 ◽

1982 ◽

Vol 21 (10) ◽

pp. 777-778 ◽

Cited By ~ 11

Author(s):

Johann Mulzer ◽

Alexander Chucholowski

Keyword(s):

Aldol Additions

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Catalytic, Enantioselective Acetone Aldol Additions with 2-Methoxypropene

Journal of the American Chemical Society ◽

10.1021/ja00117a049 ◽

1995 ◽

Vol 117 (12) ◽

pp. 3649-3650 ◽

Cited By ~ 148

Author(s):

Erick M. Carreira ◽

Wheeseong Lee ◽

Robert A. Singer

Keyword(s):

Aldol Additions

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ChemInform Abstract: Catalytic, Enantioselective Acetate Aldol Additions to α,β-Ynals: Preparation of Optically Active Propargylic Alcohols.

ChemInform ◽

10.1002/chin.199840085 ◽

2010 ◽

Vol 29 (40) ◽

pp. no-no

Author(s):

R. A. SINGER ◽

M. S. SHEPARD ◽

E. M. CARREIRA

Keyword(s):

Optically Active ◽

Propargylic Alcohols ◽

Aldol Additions

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Fundamentals and Transition-state Models. Aldol Additions of Group 1 and 2 Enolates

Modern Aldol Reactions ◽

10.1002/9783527619566.ch1 ◽

2008 ◽

pp. 1-61 ◽

Cited By ~ 10

Author(s):

Manfred Braun

Keyword(s):

Transition State ◽

Aldol Additions ◽

State Models ◽

Group 1

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Lewis Base Catalyzed Aldol Additions

Category 5, Compounds with One Saturated Carbon Heteroatom Bond ◽

10.1055/sos-sd-036-00695 ◽

2008 ◽

pp. 1

Author(s):

R. Mahrwald ◽

B. Schetter

Keyword(s):

Lewis Base ◽

Aldol Additions

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Enzyme-Catalyzed Aldol Additions

Category 5, Compounds with One Saturated Carbon Heteroatom Bond ◽

10.1055/sos-sd-036-00694 ◽

2008 ◽

pp. 1

Author(s):

R. Mahrwald ◽

B. Schetter

Keyword(s):

Aldol Additions

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Antibody-Catalyzed Aldol Additions

Category 5, Compounds with One Saturated Carbon Heteroatom Bond ◽

10.1055/sos-sd-036-00693 ◽

2008 ◽

pp. 1

Author(s):

R. Mahrwald ◽

B. Schetter

Keyword(s):

Aldol Additions

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