Tandem Sakurai-Aldol Addition Reactions as a Route to Structurally Complex Carbocycles

Benjamin D. Stevens; Scott G. Nelson

doi:10.1021/jo050225y

Tandem Sakurai-Aldol Addition Reactions as a Route to Structurally Complex Carbocycles

The Journal of Organic Chemistry ◽

10.1021/jo050225y ◽

2005 ◽

Vol 70 (11) ◽

pp. 4375-4379 ◽

Cited By ~ 17

Author(s):

Benjamin D. Stevens ◽

Scott G. Nelson

Keyword(s):

Addition Reactions ◽

Aldol Addition

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Indirect Catalytic Aldol Addition Reactions

Water in Organic Synthesis ◽

10.1055/sos-sd-206-00267 ◽

2012 ◽

pp. 1

Author(s):

M. Woyciechowska ◽

O. El-Sepelgy ◽

J. Mlynarski

Keyword(s):

Addition Reactions ◽

Aldol Addition

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ChemInform Abstract: Advances in Catalytic, Enantioselective Aldol Addition Reactions with Novel Ti(IV) Complexes

ChemInform ◽

10.1002/chin.199708271 ◽

2010 ◽

Vol 28 (8) ◽

pp. no-no

Author(s):

E. M. CARREIRA ◽

R. A. SINGER

Keyword(s):

Addition Reactions ◽

Aldol Addition

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ChemInform Abstract: Stereoselective Aldol Addition Reactions of Fischer Carbene Complexes via Electronic Tuning of the Metal Center for Enolate Reactivity.

ChemInform ◽

10.1002/chin.199446203 ◽

2010 ◽

Vol 25 (46) ◽

pp. no-no

Author(s):

W. D. WULFF ◽

B. A. ANDERSON ◽

A. J. TOOLE ◽

Y.-C. XU

Keyword(s):

Metal Center ◽

Addition Reactions ◽

Fischer Carbene Complexes ◽

Carbene Complexes ◽

Fischer Carbene ◽

Electronic Tuning ◽

Aldol Addition

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ChemInform Abstract: A Comparative Study of Solid State and Solution Aldol Addition Reactions of the Lithium Enolate of Methyl 3,3-Dimethylbutanoate: Stereochemistry and Mechanistic Implications.

ChemInform ◽

10.1002/chin.199330062 ◽

2010 ◽

Vol 24 (30) ◽

pp. no-no

Author(s):

Y. WEI ◽

R. BAKTHAVATCHALAM

Keyword(s):

Solid State ◽

Comparative Study ◽

Addition Reactions ◽

Lithium Enolate ◽

Aldol Addition

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A comparative study of solid state and solution aldol addition reactions of the lithium enolate of methyl 3,3-dimethylbutanoate: stereochemistry and mechanistic implications

Tetrahedron ◽

10.1016/s0040-4020(01)86317-1 ◽

1993 ◽

Vol 49 (12) ◽

pp. 2373-2390 ◽

Cited By ~ 3

Author(s):

Yen Wei ◽

R. Bakthavatchalam

Keyword(s):

Solid State ◽

Comparative Study ◽

Addition Reactions ◽

Lithium Enolate ◽

Aldol Addition

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ChemInform Abstract: 1,5-Asymmetric Induction in Methyl Ketone Aldol Addition Reactions.

ChemInform ◽

10.1002/chin.199726038 ◽

2010 ◽

Vol 28 (26) ◽

pp. no-no

Author(s):

D. A. EVANS ◽

P. J. COLEMAN ◽

B. COTE

Keyword(s):

Methyl Ketone ◽

Asymmetric Induction ◽

Addition Reactions ◽

Aldol Addition ◽

Methyl Ketone Aldol

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Lewis Base Activation of Lewis Acids: Catalytic, Enantioselective Vinylogous Aldol Addition Reactions

The Journal of Organic Chemistry ◽

10.1021/jo070638u ◽

2007 ◽

Vol 72 (15) ◽

pp. 5668-5688 ◽

Cited By ~ 85

Author(s):

Scott E. Denmark ◽

John R. Heemstra

Keyword(s):

Lewis Acids ◽

Lewis Base ◽

Addition Reactions ◽

Aldol Addition

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Total Synthesis of Macrolactin A with Versatile Catalytic, Enantioselective Dienolate Aldol Addition Reactions

Angewandte Chemie International Edition ◽

10.1002/(sici)1521-3773(19980518)37:9<1261::aid-anie1261>3.0.co;2-2 ◽

1998 ◽

Vol 37 (9) ◽

pp. 1261-1263 ◽

Cited By ~ 79

Author(s):

Yuntae Kim ◽

Robert A. Singer ◽

Erick M. Carreira

Keyword(s):

Total Synthesis ◽

Addition Reactions ◽

Macrolactin A ◽

Aldol Addition

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1,5-Asymmetric Induction in Boron-Mediated β-Alkoxy Methyl Ketone Aldol Addition Reactions.

ChemInform ◽

10.1002/chin.200402099 ◽

2004 ◽

Vol 35 (2) ◽

Author(s):

David A. Evans ◽

Bernard Cote ◽

Paul J. Coleman ◽

Brian T. Connell

Keyword(s):

Methyl Ketone ◽

Asymmetric Induction ◽

Addition Reactions ◽

Aldol Addition ◽

Methyl Ketone Aldol

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Lewis Base Activation of Lewis Acids. Vinylogous Aldol Addition Reactions of Conjugated N,O-Silyl Ketene Acetals to Aldehydes.

ChemInform ◽

10.1002/chin.200624030 ◽

2006 ◽

Vol 37 (24) ◽

Author(s):

Scott E. Denmark ◽

John R. Jr. Heemstra

Keyword(s):

Lewis Acids ◽

Lewis Base ◽

Addition Reactions ◽

Ketene Acetals ◽

Silyl Ketene Acetals ◽

Aldol Addition

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