Enantioselective Addition of Enol Silyl Ethers to Imines Catalyzed by Palladium Complexes:  A Novel Way to Optically Active Acylalanine Derivatives

Emiko Hagiwara; Akio Fujii; Mikiko Sodeoka

doi:10.1021/ja973962n

Enantioselective Addition of Enol Silyl Ethers to Imines Catalyzed by Palladium Complexes: A Novel Way to Optically Active Acylalanine Derivatives

Journal of the American Chemical Society ◽

10.1021/ja973962n ◽

1998 ◽

Vol 120 (10) ◽

pp. 2474-2475 ◽

Cited By ~ 166

Author(s):

Emiko Hagiwara ◽

Akio Fujii ◽

Mikiko Sodeoka

Keyword(s):

Palladium Complexes ◽

Optically Active ◽

Silyl Ethers ◽

Enantioselective Addition ◽

Enol Silyl Ethers

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ChemInform Abstract: Enantioselective Addition of Enol Silyl Ethers to Imines Catalyzed by Palladium Complexes: A Novel Way to Optically Active Acylalanine Derivatives.

ChemInform ◽

10.1002/chin.199829239 ◽

2010 ◽

Vol 29 (29) ◽

pp. no-no

Author(s):

E. HAGIWARA ◽

A. FUJII ◽

M. SODEOKA

Keyword(s):

Palladium Complexes ◽

Optically Active ◽

Silyl Ethers ◽

Enantioselective Addition ◽

Enol Silyl Ethers

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Asymmetric Michael addition of silyl nitronates to cyclic α,β-unsaturated ketones catalyzed by chiral quaternary ammonium bifluorides: isolation and selective functionalization of enol silyl ethers of optically active γ-nitro ketones

Tetrahedron Letters ◽

10.1016/j.tetlet.2005.10.154 ◽

2006 ◽

Vol 47 (2) ◽

pp. 145-148 ◽

Cited By ~ 29

Author(s):

Takashi Ooi ◽

Kanae Doda ◽

Saki Takada ◽

Keiji Maruoka

Keyword(s):

Michael Addition ◽

Quaternary Ammonium ◽

Optically Active ◽

Silyl Ethers ◽

Unsaturated Ketones ◽

Selective Functionalization ◽

Silyl Nitronates ◽

Asymmetric Michael Addition ◽

Enol Silyl Ethers

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Enantioselective Addition of Cyclic Enol Silyl Ethers to 2-Alkenoyl-Pyridine-N-Oxides Catalysed by CuII-Bis(oxazoline) Complexes

Chemistry - A European Journal ◽

10.1002/chem.201201214 ◽

2012 ◽

Vol 18 (37) ◽

pp. 11662-11668 ◽

Cited By ~ 23

Author(s):

Alessandro Livieri ◽

Massimo Boiocchi ◽

Giovanni Desimoni ◽

Giuseppe Faita

Keyword(s):

Silyl Ethers ◽

Enantioselective Addition ◽

Enol Silyl Ethers

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Highly Enantioselective Michael Addition of Silyl Nitronates to α,β-Unsaturated Aldehydes Catalyzed by Designer Chiral Ammonium Bifluorides: Efficient Access to Optically Active γ-Nitro Aldehydes and Their Enol Silyl Ethers

Journal of the American Chemical Society ◽

10.1021/ja0352810 ◽

2003 ◽

Vol 125 (30) ◽

pp. 9022-9023 ◽

Cited By ~ 73

Author(s):

Takashi Ooi ◽

Kanae Doda ◽

Keiji Maruoka

Keyword(s):

Michael Addition ◽

Optically Active ◽

Silyl Ethers ◽

Unsaturated Aldehydes ◽

Silyl Nitronates ◽

Efficient Access ◽

Enol Silyl Ethers

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Highly Enantioselective Michael Addition of Silyl Nitronates to α,β-Unsaturated Aldehydes Catalyzed by Designer Chiral Ammonium Bifluorides: Efficient Access to Optically Active γ-Nitro Aldehydes and Their Enol Silyl Ethers.

ChemInform ◽

10.1002/chin.200345033 ◽

2003 ◽

Vol 34 (45) ◽

Author(s):

Takashi Ooi ◽

Kanae Doda ◽

Keiji Maruoka

Keyword(s):

Michael Addition ◽

Optically Active ◽

Silyl Ethers ◽

Unsaturated Aldehydes ◽

Silyl Nitronates ◽

Efficient Access ◽

Enol Silyl Ethers

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Asymmetric Michael Addition of Silyl Nitronates to Cyclic α,β-Unsaturated Ketones Catalyzed by Chiral Quaternary Ammonium Bifluorides: Isolation and Selective Functionalization of Enol Silyl Ethers of Optically Active γ-Nitro Ketones.

ChemInform ◽

10.1002/chin.200617066 ◽

2006 ◽

Vol 37 (17) ◽

Author(s):

Takashi Ooi ◽

Kanae Doda ◽

Saki Takada ◽

Keiji Maruoka

Keyword(s):

Michael Addition ◽

Quaternary Ammonium ◽

Optically Active ◽

Silyl Ethers ◽

Unsaturated Ketones ◽

Selective Functionalization ◽

Silyl Nitronates ◽

Asymmetric Michael Addition ◽

Enol Silyl Ethers

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ChemInform Abstract: SYNTHESIS VIA SILYL ALKENYL ETHERS. XIV. A KETONE-ENONE CONVERSION VIA THE REACTION OF ENOL SILYL ETHERS WITH DDQ

Chemischer Informationsdienst ◽

10.1002/chin.197850146 ◽

1978 ◽

Vol 9 (50) ◽

Author(s):

I. RYU ◽

S. MURAI ◽

Y. HATAYAMA ◽

N. SONODA

Keyword(s):

Silyl Ethers ◽

Enol Silyl Ethers

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Exploiting Transient Radical Cations as Brønsted Acids for Allylic C−H Heteroarylation of Enol Silyl Ethers

Chemistry - A European Journal ◽

10.1002/chem.202101352 ◽

2021 ◽

Author(s):

Tsubasa Nakashima ◽

Haruka Fujimori ◽

Kohsuke Ohmatsu ◽

Takashi Ooi

Keyword(s):

Radical Cations ◽

Bronsted Acids ◽

Silyl Ethers ◽

Enol Silyl Ethers

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ChemInform Abstract: FLUORIDE ION CATALYZED ALDOL REACTION BETWEEN ENOL SILYL ETHERS AND CARBONYL COMPOUNDS

Chemischer Informationsdienst ◽

10.1002/chin.198339110 ◽

1983 ◽

Vol 14 (39) ◽

Author(s):

E. NAKAMURA ◽

M. SHIMIZU ◽

I. KUWAJIMA ◽

J. SAKATA ◽

K. YOKOYAMA ◽

...

Keyword(s):

Carbonyl Compounds ◽

Aldol Reaction ◽

Fluoride Ion ◽

Silyl Ethers ◽

Enol Silyl Ethers

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[3+2] Cycloaddition of 2-Alkoxycyclopropyl Carbonyl Compounds with Enol Silyl Ethers for Functionalized Cyclopentane Formation

Synlett ◽

10.1055/s-1991-20868 ◽

1991 ◽

Vol 1991 (11) ◽

pp. 771-773 ◽

Cited By ~ 46

Author(s):

Makoto Komatsu ◽

Ichiro Suehiro ◽

Yoshiaki Horiguchi ◽

Isao Kuwajima

Keyword(s):

Carbonyl Compounds ◽

Silyl Ethers ◽

Enol Silyl Ethers

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