Horseradish Peroxidase-Catalyzed Enantioselective Reduction of Racemic Hydroperoxy Homoallylic Alcohols:  A Novel Enzymatic Method for the Preparation of Optically Active, Unsaturated Diols and Hydroperoxy Alcohols

Waldemar Adam; Michael Lazarus; Ute Hoch; Marion N. Korb; Chantu R. Saha-Möller; Peter Schreier

doi:10.1021/jo980028h

Horseradish Peroxidase-Catalyzed Enantioselective Reduction of Racemic Hydroperoxy Homoallylic Alcohols: A Novel Enzymatic Method for the Preparation of Optically Active, Unsaturated Diols and Hydroperoxy Alcohols

The Journal of Organic Chemistry ◽

10.1021/jo980028h ◽

1998 ◽

Vol 63 (18) ◽

pp. 6123-6127 ◽

Cited By ~ 17

Author(s):

Waldemar Adam ◽

Michael Lazarus ◽

Ute Hoch ◽

Marion N. Korb ◽

Chantu R. Saha-Möller ◽

...

Keyword(s):

Horseradish Peroxidase ◽

Optically Active ◽

Enzymatic Method ◽

Enantioselective Reduction ◽

Homoallylic Alcohols

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ChemInform Abstract: Horseradish Peroxidase (HRP)-Catalyzed Enantioselective Reduction of Racemic Hydroperoxy Homoallylic Alcohols: A Novel Enzymatic Method for the Preparation of Optically Active, Unsaturated Diols and Hydroperoxy Alcohols.

ChemInform ◽

10.1002/chin.199724082 ◽

2010 ◽

Vol 28 (24) ◽

pp. no-no

Author(s):

W. ADAM ◽

U. HOCH ◽

H.-U. HUMPF ◽

C. R. SAHA-MOELLER ◽

P. SCHREIER

Keyword(s):

Horseradish Peroxidase ◽

Optically Active ◽

Enzymatic Method ◽

Enantioselective Reduction ◽

Homoallylic Alcohols

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ChemInform Abstract: Horseradish Peroxidase-Catalyzed Enantioselective Reduction of Racemic Hydroperoxy Homoallylic Alcohols: A Novel Enzymatic Method for the Preparation of Optically Active, Unsaturated Diols and Hydroperoxy Alcohols.

ChemInform ◽

10.1002/chin.199905042 ◽

2010 ◽

Vol 30 (5) ◽

pp. no-no

Author(s):

W. ADAM ◽

M. LAZARUS ◽

U. HOCH ◽

M. N. KORB ◽

C. R. SAHA-MOELLER ◽

...

Keyword(s):

Horseradish Peroxidase ◽

Optically Active ◽

Enzymatic Method ◽

Enantioselective Reduction ◽

Homoallylic Alcohols

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Horseradish peroxidase (HRP)-catalysed enantioselective reduction of racemic hydroperoxy homoallylic alcohols: a novel enzymatic method for the preparation of optically active, unsaturated diols and hydroperoxy alcohols

Chemical Communications ◽

10.1039/cc9960002701 ◽

1996 ◽

pp. 2701-2702 ◽

Cited By ~ 10

Author(s):

Waldemar Adam ◽

Ute Hoch ◽

Hans-Ulrich Humpf ◽

Chantu R. Saha-Möller ◽

Peter Schreier

Keyword(s):

Horseradish Peroxidase ◽

Optically Active ◽

Enzymatic Method ◽

Enantioselective Reduction ◽

Homoallylic Alcohols

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ChemInform Abstract: ASYMMETRIC SYNTHESIS VIA ACETAL TEMPLATES. 3. ON THE STEREOCHEMISTRY OBSERVED D IN THE CYCLIZATION OF CHIRAL ACETALS OF POLYOLEFINIC ALDEHYDES; FORMATION OF OPTICALLY ACTIVE HOMOALLYLIC ALCOHOLS

Chemischer Informationsdienst ◽

10.1002/chin.198328085 ◽

1983 ◽

Vol 14 (28) ◽

Author(s):

P. A. BARTLETT ◽

W. S. JOHNSON ◽

J. D. ELLIOTT

Keyword(s):

Asymmetric Synthesis ◽

Optically Active ◽

Homoallylic Alcohols

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Highly enantioselective reduction of 3-chloro-2-oxoalkanoates with fermenting bakers' yeast. A new synthesis of optically active 3-chloro-2-hydroxyalkanoates and glycidic esters

The Journal of Organic Chemistry ◽

10.1021/jo00054a036 ◽

1993 ◽

Vol 58 (2) ◽

pp. 486-492 ◽

Cited By ~ 43

Author(s):

Sadao Tsuboi ◽

Hiroyuki Furutani ◽

Mohammad Hafeez Ansari ◽

Takashi Sakai ◽

Masanori Utaka ◽

...

Keyword(s):

Optically Active ◽

Enantioselective Reduction ◽

New Synthesis

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Enantioselective Reduction of Ketones with Sodium Borohydride, Catalyzed by Optically Active(β-Oxoaldiminato)cobalt(II) Complexes

Angewandte Chemie International Edition in English ◽

10.1002/anie.199521451 ◽

1995 ◽

Vol 34 (19) ◽

pp. 2145-2147 ◽

Cited By ~ 106

Author(s):

Takushi Nagata ◽

Kiyotaka Yorozu ◽

Tohru Yamada ◽

Teruaki Mukaiyama

Keyword(s):

Sodium Borohydride ◽

Optically Active ◽

Enantioselective Reduction ◽

Reduction Of Ketones

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Asymmetric synthesis via acetal templates. 3. On the stereochemistry observed in the cyclization of chiral acetals of polyolefinic aldehydes; formation of optically active homoallylic alcohols

Journal of the American Chemical Society ◽

10.1021/ja00345a082 ◽

1983 ◽

Vol 105 (7) ◽

pp. 2088-2089 ◽

Cited By ~ 144

Author(s):

Paul A. Bartlett ◽

William S. Johnson ◽

John D. Elliott

Keyword(s):

Asymmetric Synthesis ◽

Optically Active ◽

Homoallylic Alcohols

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Asymmetric Synthesis of Optically Active Spirocyclic Indoline Scaffolds through an Enantioselective Reduction of Indoles

Chemistry - A European Journal ◽

10.1002/chem.201605450 ◽

2016 ◽

Vol 23 (4) ◽

pp. 798-801 ◽

Cited By ~ 12

Author(s):

Ruediger Borrmann ◽

Nils Knop ◽

Magnus Rueping

Keyword(s):

Asymmetric Synthesis ◽

Optically Active ◽

Enantioselective Reduction

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Asymmetric synthesis of optically active halohydrins and oxiranes by enantioselective reduction of prochiral α-haloketones with chirally modified lithium borohydride

Journal of Organometallic Chemistry ◽

10.1016/0022-328x(85)87441-6 ◽

1985 ◽

Vol 290 (2) ◽

pp. c23-c25 ◽

Cited By ~ 5

Author(s):

Kenso Soai ◽

Takashi Yamanoi ◽

Hitoshi Hikima

Keyword(s):

Asymmetric Synthesis ◽

Optically Active ◽

Lithium Borohydride ◽

Enantioselective Reduction

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Enantioselective reduction of ketones in optically active host compounds with a BH3–ethylenediamine complex in the solid state

Journal of the Chemical Society Chemical Communications ◽

10.1039/c39890001245 ◽

1989 ◽

pp. 1245-1246 ◽

Cited By ~ 25

Author(s):

Fumio Tada ◽

Koji Mori

Keyword(s):

Solid State ◽

Optically Active ◽

Enantioselective Reduction ◽

Ethylenediamine Complex ◽

Reduction Of Ketones

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