Asymmetric reduction of prochiral aromatic ketones with reagents prepared from sodium borohydride and Lewis acids in the presence of 1,2:5,6-di-O-iso-propylidene-α-D-glucofuranose

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39790000807 ◽

1979 ◽

pp. 807-808 ◽

Cited By ~ 18

Author(s):

Akira Hirao ◽

Seiichi Nakahama ◽

Didenori Mochizuki ◽

Sinichi Itsuno ◽

Masaki Ohowa ◽

...

Keyword(s):

Sodium Borohydride ◽

Lewis Acids ◽

Asymmetric Reduction ◽

Aromatic Ketones

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ChemInform Abstract: ASYMMETRIC REDUCTION OF PROCHIRAL AROMATIC KETONES WITH REAGENTS PREPARED FROM SODIUM BOROHYDRIDE AND LEWIS ACIDS IN THE PRESENCE OF 1,2:5,6-DI-O-ISOPROPYLIDENE-α-D-GLUCOFURANOSE

Chemischer Informationsdienst ◽

10.1002/chin.198006143 ◽

1980 ◽

Vol 11 (6) ◽

Author(s):

A. HIRAO ◽

S. NAKAHAMA ◽

D. MOCHIZUKI ◽

S. ITSUNO ◽

M. OHOWA ◽

...

Keyword(s):

Sodium Borohydride ◽

Lewis Acids ◽

Asymmetric Reduction ◽

Aromatic Ketones

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ChemInform Abstract: ASYMMETRIC REDUCTION OF AROMATIC KETONES WITH REAGENTS PREPARED FROM SODIUM BOROHYDRIDE AND VARIOUS CARBOXYLIC ACIDS IN THE PRESENCE OF 1,2:5,6-DI-O-ISOPROPYLIDENE-α-D-GLUCOFURANOSE

Chemischer Informationsdienst ◽

10.1002/chin.198123101 ◽

1981 ◽

Vol 12 (23) ◽

Author(s):

A. HIRAO ◽

S. ITSUNO ◽

M. OWA ◽

S. NAGAMI ◽

H. MOCHIZUKI ◽

...

Keyword(s):

Carboxylic Acids ◽

Sodium Borohydride ◽

Asymmetric Reduction ◽

Aromatic Ketones

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Asymmetric reduction of prochiral aromatic ketones with modified reagents prepared from sodium borohydride and carboxylic acids in the presence of 1,2:5,6-di-O-isopropylidene-.alpha.-D-glucofuranose

The Journal of Organic Chemistry ◽

10.1021/jo01309a036 ◽

1980 ◽

Vol 45 (21) ◽

pp. 4231-4233 ◽

Cited By ~ 29

Author(s):

Akira Hirao ◽

Seiichi Nakahama ◽

Hidenori Mochizuki ◽

Shinichi Itsuno ◽

Noboru Yamazaki

Keyword(s):

Carboxylic Acids ◽

Sodium Borohydride ◽

Asymmetric Reduction ◽

Aromatic Ketones

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Asymmetric reduction of aromatic ketones with chirally modified reagents prepared from sodium borohydride and optically active acids in the presence of 1,2:5,6-di-O-isopropylidene-.ALPHA.-D-glucofuranose.

Agricultural and Biological Chemistry ◽

10.1271/bbb1961.45.693 ◽

1981 ◽

Vol 45 (3) ◽

pp. 693-697 ◽

Cited By ~ 7

Author(s):

Akira HIRAO ◽

Hidenori MOCHIZUKI ◽

Hanafi H. Ali ZOOROB ◽

Ichiro IGARASHI ◽

Shinichi ITSUNO ◽

...

Keyword(s):

Sodium Borohydride ◽

Asymmetric Reduction ◽

Optically Active ◽

Aromatic Ketones

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Asymmetric reduction of aromatic ketones with reagents prepared from sodium borohydride and various carboxylic acids in the presence of 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose

Journal of the Chemical Society Perkin Transactions 1 ◽

10.1039/p19810000900 ◽

1981 ◽

pp. 900-905 ◽

Cited By ~ 22

Author(s):

Akira Hirao ◽

Shinichi Itsuno ◽

Masaki Owa ◽

Satoru Nagami ◽

Hidenori Mochizuki ◽

...

Keyword(s):

Carboxylic Acids ◽

Sodium Borohydride ◽

Asymmetric Reduction ◽

Aromatic Ketones

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ChemInform Abstract: ASYMMETRIC REDUCTION OF PROCHIRAL AROMATIC KETONES WITH MODIFIED REAGENTS PREPARED FROM SODIUM BOROHYDRIDE AND CARBOXYLIC ACIDS IN THE PRESENCE OF 1,2:5,6-DI-O-ISOPROPYLIDENE-A-D-GLUCOFURANOSE

Chemischer Informationsdienst ◽

10.1002/chin.198107163 ◽

1981 ◽

Vol 12 (7) ◽

Author(s):

A. HIRAO ◽

S. NAKAHAMA ◽

H. MOCHIZUKI ◽

S. ITSUNO ◽

N. YAMAZAKI

Keyword(s):

Carboxylic Acids ◽

Sodium Borohydride ◽

Asymmetric Reduction ◽

Aromatic Ketones

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Asymmetric Reduction of Aromatic Ketones with Chirally Modified Reagents Prepared from Sodium Borohydride and Optically Active Acids in the Presence of l,2:5,6-Di-0-isopropylidene- α-d-glucofuranose

Agricultural and Biological Chemistry ◽

10.1080/00021369.1981.10864567 ◽

1981 ◽

Vol 45 (3) ◽

pp. 693-697 ◽

Cited By ~ 1

Author(s):

Akira Hirao ◽

Hidenori Mochizuki ◽

Hanafi H. Ali Zoorob ◽

Ichiro Igarashi ◽

Shinichi Itsuno ◽

...

Keyword(s):

Sodium Borohydride ◽

Asymmetric Reduction ◽

Optically Active ◽

Aromatic Ketones

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Asymmetric reduction of aromatic ketones by sodium borohydride in the presence of bovine serum albumin

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39780000926 ◽

1978 ◽

pp. 926 ◽

Cited By ~ 27

Author(s):

Toyonari Sugimoto ◽

Yasuo Matsumura ◽

Shigeo Tanimoto ◽

Masaya Okano

Keyword(s):

Bovine Serum Albumin ◽

Serum Albumin ◽

Sodium Borohydride ◽

Bovine Serum ◽

Asymmetric Reduction ◽

Aromatic Ketones

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A Mild, Enantioselective Synthesis of (R)-Salmeterol via Sodium Borohydride—Calcium Chloride Asymmetric Reduction of a Phenacyl Phenylglycinol Derivative.

ChemInform ◽

10.1002/chin.200306084 ◽

2003 ◽

Vol 34 (6) ◽

Author(s):

Robert N. Bream ◽

Steven V. Ley ◽

Benjamin McDermott ◽

Panayiotis A. Procopiou

Keyword(s):

Calcium Chloride ◽

Sodium Borohydride ◽

Asymmetric Reduction ◽

Enantioselective Synthesis

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Synthesis of a new class of ligands derived from isosorbide and their application to asymmetric reduction of aromatic ketones by transfer hydrogenation

New Journal of Chemistry ◽

10.1039/c1nj20588a ◽

2011 ◽

Vol 35 (11) ◽

pp. 2622 ◽

Cited By ~ 19

Author(s):

Khanh-Duy Huynh ◽

Houssein Ibrahim ◽

Emile Kolodziej ◽

Martial Toffano ◽

Giang Vo-Thanh

Keyword(s):

Asymmetric Reduction ◽

Transfer Hydrogenation ◽

Aromatic Ketones ◽

New Class

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