Access to enantiomerically pure intermediates for (−)-geosmin synthesis starting from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methyl-naphthalen-2(3H)-one

Ken Ichi Fuhshuku; Takeshi Sugai

doi:10.1271/bbb.66.2267

Access to enantiomerically pure intermediates for (−)-geosmin synthesis starting from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methyl-naphthalen-2(3H)-one

Ken Ichi Fuhshuku, Takeshi Sugai

School of Pharmaceutical Sciences

Research output: Contribution to journal › Article › peer-review

5 Citations (Scopus)

Abstract

Enantiomerically pure key intermediates for the synthesis of the natural enantiomer of geosmin were synthesized from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3H)-one.

Original language	English
Pages (from-to)	2267-2272
Number of pages	6
Journal	Bioscience, Biotechnology and Biochemistry
Volume	66
Issue number	10
DOIs	https://doi.org/10.1271/bbb.66.2267
Publication status	Published - 2002 Jan 1

Keywords

Cyclopropanation
Geosmin
Hydrogenation
Wieland-Miescher ketone

ASJC Scopus subject areas

Biotechnology
Analytical Chemistry
Biochemistry
Applied Microbiology and Biotechnology
Molecular Biology
Organic Chemistry

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10.1271/bbb.66.2267

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abstract = "Enantiomerically pure key intermediates for the synthesis of the natural enantiomer of geosmin were synthesized from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3H)-one.",

keywords = "Cyclopropanation, Geosmin, Hydrogenation, Wieland-Miescher ketone",

author = "Fuhshuku, {Ken Ichi} and Takeshi Sugai",

year = "2002",

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doi = "10.1271/bbb.66.2267",

language = "English",

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journal = "Bioscience, Biotechnology and Biochemistry",

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T1 - Access to enantiomerically pure intermediates for (−)-geosmin synthesis starting from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methyl-naphthalen-2(3H)-one

AU - Fuhshuku, Ken Ichi

AU - Sugai, Takeshi

PY - 2002/1/1

Y1 - 2002/1/1

N2 - Enantiomerically pure key intermediates for the synthesis of the natural enantiomer of geosmin were synthesized from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3H)-one.

AB - Enantiomerically pure key intermediates for the synthesis of the natural enantiomer of geosmin were synthesized from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3H)-one.

KW - Cyclopropanation

KW - Geosmin

KW - Hydrogenation

KW - Wieland-Miescher ketone

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JO - Bioscience, Biotechnology and Biochemistry

JF - Bioscience, Biotechnology and Biochemistry

IS - 10

ER -

Access to enantiomerically pure intermediates for (−)-geosmin synthesis starting from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methyl-naphthalen-2(3H)-one

Abstract

Keywords

ASJC Scopus subject areas

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