ChemInform Abstract: Effective and Mild Method for Preparation of Optically Active α-Amino Aldehydes via TEMPO Oxidation.

J. JURCZAK; D. GRYKO; E. KOBRZYCKA; H. GRUZA; P. PROKOPOWICZ

doi:10.1002/chin.199836113

ChemInform Abstract: Effective and Mild Method for Preparation of Optically Active α-Amino Aldehydes via TEMPO Oxidation.

ChemInform ◽

10.1002/chin.199836113 ◽

2010 ◽

Vol 29 (36) ◽

pp. no-no

Author(s):

J. JURCZAK ◽

D. GRYKO ◽

E. KOBRZYCKA ◽

H. GRUZA ◽

P. PROKOPOWICZ

Keyword(s):

Optically Active ◽

Tempo Oxidation ◽

Amino Aldehydes

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Effective and mild method for preparation of optically active α-amino aldehydes via TEMPO oxidation

Tetrahedron ◽

10.1016/s0040-4020(98)00299-3 ◽

1998 ◽

Vol 54 (22) ◽

pp. 6051-6064 ◽

Cited By ~ 54

Author(s):

Janusz Jurczak ◽

Dorota Gryko ◽

Elżbieta Kobrzycka ◽

Henryk Gruza ◽

Piotr Prokopowicz

Keyword(s):

Optically Active ◽

Tempo Oxidation ◽

Amino Aldehydes

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Stereospecific Rearrangement of Optically Active Tertiary Allylic Epoxides To Give Optically Active Quaternary Aldehydes: Synthesis of .alpha.-Alkyl Amino Aldehydes and Acids

Journal of the American Chemical Society ◽

10.1021/ja00133a011 ◽

1995 ◽

Vol 117 (28) ◽

pp. 7379-7388 ◽

Cited By ~ 79

Author(s):

Michael E. Jung ◽

Derin C. D'Amico

Keyword(s):

Optically Active ◽

Amino Aldehydes

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Gold(I)-Catalyzed Asymmetric Aldol Reaction of N-Methoxy-N-methyl-.alpha.-isocyanoacetamide (.alpha.-Isocyano Weinreb Amide). An Efficient Synthesis of Optically Active .beta.-Hydroxy .alpha.-Amino Aldehydes and Ketones

The Journal of Organic Chemistry ◽

10.1021/jo00111a034 ◽

1995 ◽

Vol 60 (6) ◽

pp. 1727-1732 ◽

Cited By ~ 82

Author(s):

Masaya Sawamura ◽

Yuki Nakayama ◽

Tomoki Kato ◽

Yoshihiko Ito

Keyword(s):

Aldol Reaction ◽

Optically Active ◽

Efficient Synthesis ◽

Asymmetric Aldol ◽

Amino Aldehydes ◽

Weinreb Amide ◽

Asymmetric Aldol Reaction ◽

Aldehydes And Ketones

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ChemInform Abstract: Gold(I)-Catalyzed Asymmetric Aldol Reaction of N-Methoxy-N-methyl-. alpha.-isocyanoacetamide (α-Isocyano Weinreb Amide) (I). An Efficient Synthesis of Optically Active β-Hydroxy α-Amino Aldehydes (VIII) and Ketones (X).

ChemInform ◽

10.1002/chin.199535044 ◽

2010 ◽

Vol 26 (35) ◽

pp. no-no

Author(s):

M. SAWAMURA ◽

Y. NAKAYAMA ◽

T. KATO ◽

Y. ITO

Keyword(s):

Aldol Reaction ◽

Optically Active ◽

Efficient Synthesis ◽

Asymmetric Aldol ◽

Amino Aldehydes ◽

Weinreb Amide ◽

Asymmetric Aldol Reaction

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ChemInform Abstract: Stereospecific Rearrangement of Optically Active Tertiary Allylic Epoxides to Give Optically Active Quaternary Aldehydes: Synthesis of . alpha.-Alkyl Amino Aldehydes and Acids.

ChemInform ◽

10.1002/chin.199545067 ◽

2010 ◽

Vol 26 (45) ◽

pp. no-no

Author(s):

M. E. JUNG ◽

D. C. D'AMICO

Keyword(s):

Optically Active ◽

Amino Aldehydes

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ChemInform Abstract: NEW METHODS AND REAGENTS IN ORGANIC SYNTHESIS. 29. A PRACTICAL METHOD FOR THE E PREPARATION OF OPTICALLY ACTIVE N-PROTECTED α-AMINO ALDEHYDES AND PEPTIDE ALDEHYDES

Chemischer Informationsdienst ◽

10.1002/chin.198244330 ◽

1982 ◽

Vol 13 (44) ◽

Author(s):

Y. HAMADA ◽

T. SHIOIRI

Keyword(s):

Organic Synthesis ◽

Practical Method ◽

Optically Active ◽

Amino Aldehydes ◽

New Methods ◽

Peptide Aldehydes

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Highly regio- and diastereoselective friedel-crafts alkylation of phenols with α-amino aldehydes. Synthesis of optically active ephedrine-like compounds

Tetrahedron Letters ◽

10.1016/s0040-4039(01)80376-2 ◽

1989 ◽

Vol 30 (9) ◽

pp. 1121-1124 ◽

Cited By ~ 10

Author(s):

Franca Bigi ◽

Giuseppe Casnati ◽

Giovanni Sartori ◽

Gianluca Araldi ◽

Gabriele Bocelli

Keyword(s):

Optically Active ◽

Amino Aldehydes

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ChemInform Abstract: Direct Organo-Catalytic Asymmetric α-Amination of Aldehydes - A Simple Approach to Optically Active α-Amino Aldehydes, α-Amino Alcohols, and α-Amino Acids.

ChemInform ◽

10.1002/chin.200239186 ◽

2010 ◽

Vol 33 (39) ◽

pp. no-no

Author(s):

Anders Boegevig ◽

Karsten Juhl ◽

Nagaswamy Kumaragurubaran ◽

Wei Zhuang ◽

Karl Anker Joergensen

Keyword(s):

Amino Acids ◽

Amino Alcohols ◽

Simple Approach ◽

Optically Active ◽

Amino Aldehydes ◽

Catalytic Asymmetric

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.alpha.,.beta.-Epoxy sulfoxides as useful intermediates in organic synthesis. 21. A novel approach to the asymmetric synthesis of epoxides, allylic alcohols, .alpha.-amino ketones, and .alpha.-amino aldehydes from carbonyl compounds through .alpha.,.beta.-epoxy sulfoxides using the optically active p-tolylsulfinyl group to induce chirality

The Journal of Organic Chemistry ◽

10.1021/jo00274a032 ◽

1989 ◽

Vol 54 (13) ◽

pp. 3130-3136 ◽

Cited By ~ 97

Author(s):

Tsuyoshi Satoh ◽

Teruhiko Oohara ◽

Yoshiko Ueda ◽

Koji Yamakawa

Keyword(s):

Asymmetric Synthesis ◽

Organic Synthesis ◽

Carbonyl Compounds ◽

Optically Active ◽

Allylic Alcohols ◽

Amino Aldehydes ◽

Novel Approach ◽

Alpha Beta

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Asymmetric Skeletal Rearrangement of Symmetrically α,α-Disubstituted α-Amino Aldehydes: A New Entry to Optically Active α-Hydroxy Ketones

Journal of the American Chemical Society ◽

10.1021/ja0292851 ◽

2003 ◽

Vol 125 (11) ◽

pp. 3220-3221 ◽

Cited By ~ 29

Author(s):

Takashi Ooi ◽

Akira Saito ◽

Keiji Maruoka

Keyword(s):

Optically Active ◽

Skeletal Rearrangement ◽

Amino Aldehydes ◽

Hydroxy Ketones ◽

New Entry

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