ChemInform Abstract: The Origin of π-Facial Diastereoselectivity in Nucleophilic Additions to Chiral Carbonyl Compounds. Part 3. Rotational Profiles of 2-Methoxypropanal and 2-N,N-Dimethylaminopropanal.

G. FRENKING; K. F. KOEHLER; M. T. REETZ

doi:10.1002/chin.199337076

ChemInform Abstract: The Origin of π-Facial Diastereoselectivity in Nucleophilic Additions to Chiral Carbonyl Compounds. Part 3. Rotational Profiles of 2-Methoxypropanal and 2-N,N-Dimethylaminopropanal.

ChemInform ◽

10.1002/chin.199337076 ◽

2010 ◽

Vol 24 (37) ◽

pp. no-no

Author(s):

G. FRENKING ◽

K. F. KOEHLER ◽

M. T. REETZ

Keyword(s):

Carbonyl Compounds ◽

Nucleophilic Additions ◽

Chiral Carbonyl Compounds

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On the origin of π-facial diastereoselectivity in nucleophilic additions to chiral carbonyl compounds. 1. Rotational profiles of propionaldehyde 1, chloroacetaldehyde 2, and 2-chloropropionaldehyde 3.

Tetrahedron ◽

10.1016/s0040-4020(01)86504-2 ◽

1991 ◽

Vol 47 (43) ◽

pp. 8991-9004 ◽

Cited By ~ 21

Author(s):

G Frenking ◽

K.F Köhler ◽

M.T Reetz

Keyword(s):

Carbonyl Compounds ◽

Nucleophilic Additions ◽

Chiral Carbonyl Compounds

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On the origin of π-facial diastereoselectivity in nucleophilic additions to chiral carbonyl compounds 4. Calculated transition state structures for the addition of nucleophiles to 2-methoxypropanal and 2-N,N-dimethyl-aminopropanal.

Tetrahedron ◽

10.1016/s0040-4020(01)89912-9 ◽

1993 ◽

Vol 49 (19) ◽

pp. 3983-3994 ◽

Cited By ~ 19

Author(s):

G. Frenking ◽

K.F. Köhler ◽

M.T. Reetz

Keyword(s):

Transition State ◽

Carbonyl Compounds ◽

Nucleophilic Additions ◽

Chiral Carbonyl Compounds ◽

Transition State Structures

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On the origin of π-facial diastereoselectivity in nucleophilic additions to chiral carbonyl compounds. 2. Calculated transition state structures for the addition of nucleophiles to propionaldehyde 1, chloroacetyldehyde 2, and 2-chloropropionaldehyde 3.

Tetrahedron ◽

10.1016/s0040-4020(01)86505-4 ◽

1991 ◽

Vol 47 (43) ◽

pp. 9005-9018 ◽

Cited By ~ 23

Author(s):

G Frenking ◽

K.F Köhler ◽

M.T Reetz

Keyword(s):

Transition State ◽

Carbonyl Compounds ◽

Nucleophilic Additions ◽

Chiral Carbonyl Compounds ◽

Transition State Structures

Download Full-text

ChemInform Abstract: The Origin of π-Facial Diastereoselectivity in Nucleophilic Additions to Chiral Carbonyl Compounds. Part 4. Calculated Transition State Structures for the Addition of Nucleophiles to 2-Methoxypropanal and 2-N,N-Dimethylaminopropanal.

ChemInform ◽

10.1002/chin.199337077 ◽

2010 ◽

Vol 24 (37) ◽

pp. no-no

Author(s):

G. FRENKING ◽

K. F. KOEHLER ◽

M. T. REETZ

Keyword(s):

Transition State ◽

Carbonyl Compounds ◽

Nucleophilic Additions ◽

Chiral Carbonyl Compounds ◽

Transition State Structures

Download Full-text

On the origin of π-facial diastereoselectivity in nucleophilic additions to chiral carbonyl compounds 3. Rotational profiles of 2-methoxypropanal and 2-N,N-dimethylaminopropanal.

Tetrahedron ◽

10.1016/s0040-4020(01)89911-7 ◽

1993 ◽

Vol 49 (19) ◽

pp. 3971-3982 ◽

Cited By ~ 10

Author(s):

G. Frenking ◽

K.F. Köhler ◽

M.T. Reetz

Keyword(s):

Carbonyl Compounds ◽

Nucleophilic Additions ◽

Chiral Carbonyl Compounds

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The effect of cations on nucleophilic additions to carbonyl compounds: carbonyl complexation control versus ionic association control. application to t

Tetrahedron ◽

10.1016/0040-4020(78)88393-8 ◽

1978 ◽

Vol 34 (16) ◽

pp. 2597-2605 ◽

Cited By ~ 74

Author(s):

Jean-Michel Lefour ◽

André Loupy

Keyword(s):

Carbonyl Compounds ◽

Ionic Association ◽

Nucleophilic Additions ◽

Control Versus ◽

Control Application

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Utilization of Donor-Acceptor Interactions for the Catalytic Acceleration of Nucleophilic Additions to Aromatic Carbonyl Compounds

Angewandte Chemie ◽

10.1002/ange.201711726 ◽

2018 ◽

Vol 130 (8) ◽

pp. 2152-2155 ◽

Cited By ~ 4

Author(s):

Tatsuhiro Uchikura ◽

Kosuke Ono ◽

Kohei Takahashi ◽

Nobuharu Iwasawa

Keyword(s):

Carbonyl Compounds ◽

Nucleophilic Additions ◽

Donor Acceptor ◽

Aromatic Carbonyl Compounds

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Utilization of Donor-Acceptor Interactions for the Catalytic Acceleration of Nucleophilic Additions to Aromatic Carbonyl Compounds

Angewandte Chemie International Edition ◽

10.1002/anie.201711726 ◽

2018 ◽

Vol 57 (8) ◽

pp. 2130-2133 ◽

Cited By ~ 5

Author(s):

Tatsuhiro Uchikura ◽

Kosuke Ono ◽

Kohei Takahashi ◽

Nobuharu Iwasawa

Keyword(s):

Carbonyl Compounds ◽

Nucleophilic Additions ◽

Donor Acceptor ◽

Aromatic Carbonyl Compounds

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CHAPTER 8. Synthesis of Chiral Acyclic Compounds Through Enantioselective Cobalt-catalysed 1,2-Nucleophilic Additions to Carbonyl Compounds and Derivatives

Catalysis Series - Enantioselective Cobalt-catalysed Transformations ◽

10.1039/9781788015097-00178 ◽

2018 ◽

pp. 178-187

Keyword(s):

Carbonyl Compounds ◽

Nucleophilic Additions

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ChemInform Abstract: Trimethylsilyl Cyanide - A Reagent for Umpolung. Part 17. Diastereoselectivity in Nucleophilic Acylations of α-Chiral Carbonyl Compounds with α,β-Unsaturated Aldehydes After Umpolung.

ChemInform ◽

10.1002/chin.199004104 ◽

1990 ◽

Vol 21 (4) ◽

Author(s):

S. HUENIG ◽

C. MARSCHNER ◽

K. PETERS ◽

H. G. VON SCHNERING

Keyword(s):

Carbonyl Compounds ◽

Trimethylsilyl Cyanide ◽

Unsaturated Aldehydes ◽

Chiral Carbonyl Compounds

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