.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

Tsuyoshi Satoh; Teruhiko Oohara; Yoshiko Ueda; Koji Yamakawa

doi:10.1021/jo00274a032

.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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ChemInform Abstract: α,β-Epoxy Sulfoxides as Useful Intermediates in Organic Synthesis. Part 21. A Novel Approach to the Asymmetric Synthesis of Epoxides, Allylic Alcohols, α-Amino Ketones, and α-Amino Aldehydes from Carbonyl Compounds Through α,β-Epoxy S

ChemInform ◽

10.1002/chin.198948152 ◽

1989 ◽

Vol 20 (48) ◽

Author(s):

T. SATOH ◽

T. OOHARA ◽

Y. UEDA ◽

K. YAMAKAWA

Keyword(s):

Asymmetric Synthesis ◽

Organic Synthesis ◽

Carbonyl Compounds ◽

Allylic Alcohols ◽

Amino Aldehydes ◽

Novel Approach

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ChemInform Abstract: α,β-Epoxy Sulfoxides as Useful Intermediates in Organic Synthesis. Part 17. A Novel Approach to the Synthesis of Chiral Epoxides and Allylic Alcohols by the Use of Optically Active p-Tolylsulfinyl Group as a Chiral Auxiliary.

ChemInform ◽

10.1002/chin.198846161 ◽

1988 ◽

Vol 19 (46) ◽

Author(s):

T. SATOH ◽

T. OOHARA ◽

K. YAMAKAWA

Keyword(s):

Organic Synthesis ◽

Optically Active ◽

Chiral Auxiliary ◽

Allylic Alcohols ◽

Chiral Epoxides ◽

Novel Approach

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Selective oxidation of alcohol function in allylic alcohols to .alpha.,.beta.-unsaturated carbonyl compounds catalyzed by zirconocene complexes

The Journal of Organic Chemistry ◽

10.1021/jo00231a006 ◽

1987 ◽

Vol 52 (22) ◽

pp. 4855-4859 ◽

Cited By ~ 22

Author(s):

Tatsuya Nakano ◽

Yasutaka Ishii ◽

Masaya Ogawa

Keyword(s):

Selective Oxidation ◽

Carbonyl Compounds ◽

Allylic Alcohols ◽

Alpha Beta

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.alpha.,.beta.-Epoxy sulfoxides as useful intermediates in organic synthesis. 22. Stereospecific desulfinylation of sulfinylaziridines with alkylmetals: a novel synthesis including asymmetric synthesis of (Z)-N-arylaziridines and some mechanistic studies

The Journal of Organic Chemistry ◽

10.1021/jo00277a041 ◽

1989 ◽

Vol 54 (16) ◽

pp. 3973-3978 ◽

Cited By ~ 71

Author(s):

Tsuyoshi Satoh ◽

Takahiko Sato ◽

Teruhiko Oohara ◽

Koji Yamakawa

Keyword(s):

Asymmetric Synthesis ◽

Organic Synthesis ◽

Mechanistic Studies ◽

Novel Synthesis ◽

Alpha Beta

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ChemInform Abstract: Electroreductive Coupling of Optically Active α,β-Unsaturated Carbonyl Compounds with Diaryl Ketones: Asymmetric Synthesis of 4,5,5-Trisubstituted γ-Butyrolactones.

ChemInform ◽

10.1002/chin.201450104 ◽

2014 ◽

Vol 45 (50) ◽

pp. no-no

Author(s):

Naoki Kise ◽

Yusuke Hamada ◽

Toshihiko Sakurai

Keyword(s):

Asymmetric Synthesis ◽

Carbonyl Compounds ◽

Optically Active

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ChemInform Abstract: REDUCTION OF CARBONYL COMPOUNDS VIA HYDROSILYLATION. V. SYNTHESIS OF OPTICALLY ACTIVE ALLYLIC ALCOHOLS VIA REGIOSELECTIVE ASYMMETRIC HYDROSILYLATION

Chemischer Informationsdienst ◽

10.1002/chin.198301128 ◽

1983 ◽

Vol 14 (1) ◽

Author(s):

T. KOGURE ◽

I. OJIMA

Keyword(s):

Carbonyl Compounds ◽

Optically Active ◽

Allylic Alcohols

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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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Meerwein-Ponndorf-Verley-type reduction of dicarbonyl compounds to hydroxy carbonyl compounds and .alpha.,.beta.-unsaturated carbonyl compounds to allylic alcohols catalyzed by zirconocene and hafnocene complexes

The Journal of Organic Chemistry ◽

10.1021/jo00251a016 ◽

1988 ◽

Vol 53 (16) ◽

pp. 3752-3757 ◽

Cited By ~ 40

Author(s):

Tatsuya Nakano ◽

Shigetoshi Umano ◽

Yoshio Kino ◽

Yasutaka Ishii ◽

Masaya Ogawa

Keyword(s):

Carbonyl Compounds ◽

Allylic Alcohols ◽

Dicarbonyl Compounds ◽

Type Reduction ◽

Alpha Beta

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ChemInform Abstract: α,β-Epoxy Sulfides as Useful Intermediates in Organic Synthesis. Part 6. A Novel Synthesis of Epoxides and Allylic Alcohols from Carbonyl Compounds through α,β-Epoxy Sulfoxides.

Chemischer Informationsdienst ◽

10.1002/chin.198644157 ◽

1986 ◽

Vol 17 (44) ◽

Author(s):

T. SATOH ◽

Y. KANEKO ◽

K. YAMAKAWA

Keyword(s):

Organic Synthesis ◽

Carbonyl Compounds ◽

Allylic Alcohols ◽

Novel Synthesis

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A novel approach to the synthesis of chiral epoxides and allylic alcohols by the use of optically active p-tolyl sulfinyl group as a chiral auxiliary

Tetrahedron Letters ◽

10.1016/0040-4039(88)85228-6 ◽

1988 ◽

Vol 29 (23) ◽

pp. 2851-2854 ◽

Cited By ~ 19

Author(s):

Tsuyoshi Satoh ◽

Teruhiko Oohara ◽

Koji Yamakawa

Keyword(s):

Optically Active ◽

Chiral Auxiliary ◽

Allylic Alcohols ◽

Chiral Epoxides ◽

Novel Approach ◽

Sulfinyl Group

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