CN101535286B - 色烯的对映选择性氢化方法 - Google Patents

色烯的对映选择性氢化方法 Download PDF

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Publication number
CN101535286B
CN101535286B CN200680036577.1A CN200680036577A CN101535286B CN 101535286 B CN101535286 B CN 101535286B CN 200680036577 A CN200680036577 A CN 200680036577A CN 101535286 B CN101535286 B CN 101535286B
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CN
China
Prior art keywords
phenyl
equol
chromene
compound
chroman
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN200680036577.1A
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English (en)
Chinese (zh)
Other versions
CN101535286A (zh
Inventor
K·D·R·塞特查尔
V·D·索罗金
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cincinnati Childrens Hospital Medical Center
Girindus America Inc
Original Assignee
Cincinnati Childrens Hospital Medical Center
Girindus America Inc
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Filing date
Publication date
Application filed by Cincinnati Childrens Hospital Medical Center, Girindus America Inc filed Critical Cincinnati Childrens Hospital Medical Center
Priority to CN201310655782.8A priority Critical patent/CN103755675B/zh
Priority to CN201310533995.3A priority patent/CN103641808B/zh
Publication of CN101535286A publication Critical patent/CN101535286A/zh
Application granted granted Critical
Publication of CN101535286B publication Critical patent/CN101535286B/zh
Expired - Fee Related legal-status Critical Current
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D311/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/22Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4
    • C07D311/26Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3
    • C07D311/34Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 4 with aromatic rings attached in position 2 or 3 with aromatic rings attached in position 3 only
    • C07D311/382,3-Dihydro derivatives, e.g. isoflavanones

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pyrane Compounds (AREA)
CN200680036577.1A 2005-08-01 2006-08-01 色烯的对映选择性氢化方法 Expired - Fee Related CN101535286B (zh)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201310655782.8A CN103755675B (zh) 2005-08-01 2006-08-01 色烯的对映选择性氢化方法
CN201310533995.3A CN103641808B (zh) 2005-08-01 2006-08-01 色烯的对映选择性氢化方法

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US11/194,280 US7528267B2 (en) 2005-08-01 2005-08-01 Method for enantioselective hydrogenation of chromenes
US11/194,280 2005-08-01
PCT/US2006/029589 WO2007016423A2 (en) 2005-08-01 2006-08-01 Method for enantioselective hydrogenation of chromenes

Related Child Applications (2)

Application Number Title Priority Date Filing Date
CN201310533995.3A Division CN103641808B (zh) 2005-08-01 2006-08-01 色烯的对映选择性氢化方法
CN201310655782.8A Division CN103755675B (zh) 2005-08-01 2006-08-01 色烯的对映选择性氢化方法

Publications (2)

Publication Number Publication Date
CN101535286A CN101535286A (zh) 2009-09-16
CN101535286B true CN101535286B (zh) 2014-05-07

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Family Applications (3)

Application Number Title Priority Date Filing Date
CN200680036577.1A Expired - Fee Related CN101535286B (zh) 2005-08-01 2006-08-01 色烯的对映选择性氢化方法
CN201310655782.8A Expired - Fee Related CN103755675B (zh) 2005-08-01 2006-08-01 色烯的对映选择性氢化方法
CN201310533995.3A Expired - Fee Related CN103641808B (zh) 2005-08-01 2006-08-01 色烯的对映选择性氢化方法

Family Applications After (2)

Application Number Title Priority Date Filing Date
CN201310655782.8A Expired - Fee Related CN103755675B (zh) 2005-08-01 2006-08-01 色烯的对映选择性氢化方法
CN201310533995.3A Expired - Fee Related CN103641808B (zh) 2005-08-01 2006-08-01 色烯的对映选择性氢化方法

Country Status (8)

Country Link
US (4) US7528267B2 (cg-RX-API-DMAC7.html)
EP (1) EP1919887B1 (cg-RX-API-DMAC7.html)
JP (1) JP5507081B2 (cg-RX-API-DMAC7.html)
CN (3) CN101535286B (cg-RX-API-DMAC7.html)
AU (1) AU2006275587B2 (cg-RX-API-DMAC7.html)
CA (1) CA2617665C (cg-RX-API-DMAC7.html)
DK (1) DK1919887T3 (cg-RX-API-DMAC7.html)
WO (1) WO2007016423A2 (cg-RX-API-DMAC7.html)

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EP1569636B1 (en) 2002-10-29 2017-12-13 Colorado State University Research Foundation Use of equol for treating androgen mediated diseases
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US7714348B2 (en) * 2006-10-06 2010-05-11 Ac-Led Lighting, L.L.C. AC/DC light emitting diodes with integrated protection mechanism
JP5355395B2 (ja) * 2007-06-13 2013-11-27 大塚製薬株式会社 エクオール含有抽出物及びその製造方法、エクオール抽出方法、並びにエクオールを含む食品
EP2231648A1 (en) * 2007-12-05 2010-09-29 BIAL - Portela & Ca., S.A. New salts and crystal forms
EP2133080A1 (de) 2008-06-13 2009-12-16 Haelan Schweiz GmbH Zusammensetzungen enthaltend Equol
RU2364442C1 (ru) * 2008-06-30 2009-08-20 Государственное образовательное учреждение высшего профессионального образования "Тверской государственный технический университет" Способ приготовления модифицированного платинового катализатора для энантиоселективного гидрирования сложных эфиров альфа-кетокарбоновых кислот
EP2154133A1 (de) * 2008-08-14 2010-02-17 System Biologie AG Synthese von Equol
US20110091435A1 (en) * 2008-10-24 2011-04-21 University Of Southern California Phytoestrogenic formulations for alleviation or prevention of hair loss
US7875735B2 (en) * 2009-05-19 2011-01-25 Kaohsiung Medical University Processes for preparing isoflavonoids using 7-benzyloxy-3-(4-methoxyphenyl)-2H-1-benzopyran as a starting material
US7875736B2 (en) * 2009-05-19 2011-01-25 Kaohsiung Medical University Intermediate compounds and processes for the preparation of 7-benzyloxy-3-(4-methoxyphenyl)-2H-1-benzopyran
JP5780651B2 (ja) * 2009-09-18 2015-09-16 不二製油株式会社 エクオールの不斉合成法
CN102633763B (zh) * 2012-04-11 2014-02-26 黑龙江大学 一种(s)-雌马酚的制备方法
DK2953938T3 (en) 2014-02-07 2017-10-02 Novogen ltd Functionalized benzopyran compounds and their use
DK3191464T3 (da) * 2014-09-10 2020-02-03 System Biologie Ag Syntese af isoflavaner og intermediater deraf
EP3207034B1 (en) 2014-10-14 2023-06-07 Richard L. Jackson Anhydrous crystalline form of s-equol
AU2017301596A1 (en) 2016-07-26 2019-02-07 Ausio Pharmaceuticals, Llc Methods of diagnosing and treating Alzheimer's disease with S-equol
EP3843718A1 (en) 2018-06-15 2021-07-07 The Board Of Regents Of The University Of Texas System Methods of treating and preventing melanoma with s-equol
WO2019240871A1 (en) 2018-06-15 2019-12-19 The Board Of Regents Of The University Of Texas System Methods of treating and preventing breast cancer with s-equol
KR102819124B1 (ko) * 2018-10-02 2025-06-12 주식회사 글라세움 탄소 이중결합 함유 화합물의 비대칭 수소첨가 반응용 촉매
WO2020071818A1 (ko) * 2018-10-02 2020-04-09 주식회사 글라세움 탄소 이중결합 함유 화합물의 비대칭 수소첨가 반응용 촉매

Citations (1)

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CN1340048A (zh) * 1999-02-15 2002-03-13 诺沃根研究有限公司 异黄酮衍生物的制备

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GB8626344D0 (en) * 1986-11-04 1986-12-03 Zyma Sa Bicyclic compounds
AUPO203996A0 (en) * 1996-08-30 1996-09-26 Novogen Research Pty Ltd Therapeutic uses
KR20000057548A (ko) * 1996-12-13 2000-09-25 알프레드 엘. 미첼슨 광학적 전송물질 및 결합재
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WO2001034612A2 (en) * 1999-11-10 2001-05-17 The Penn State Research Foundation Chiral phosphines, transition metal complexes thereof and uses thereof in asymmetric reactions
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Andreas Pfaltz, et. al..Iridium-Catalyzed Enantioselective Hydrogenation of Olefins.《Adv. Synth. Catal.》.2003,第345卷33-43,特别是第41页图12的Ir-B2. *

Also Published As

Publication number Publication date
WO2007016423A2 (en) 2007-02-08
US7960573B2 (en) 2011-06-14
JP5507081B2 (ja) 2014-05-28
CN103641808A (zh) 2014-03-19
CA2617665A1 (en) 2007-02-08
WO2007016423A3 (en) 2009-04-30
CN103755675A (zh) 2014-04-30
US20100069653A1 (en) 2010-03-18
US7528267B2 (en) 2009-05-05
EP1919887B1 (en) 2015-02-18
AU2006275587A1 (en) 2007-02-08
US8263790B2 (en) 2012-09-11
US20120004427A1 (en) 2012-01-05
CN103755675B (zh) 2015-11-18
US20130116450A1 (en) 2013-05-09
DK1919887T3 (en) 2015-05-26
JP2009503079A (ja) 2009-01-29
EP1919887A4 (en) 2011-01-19
US8716497B2 (en) 2014-05-06
US20070027329A1 (en) 2007-02-01
EP1919887A2 (en) 2008-05-14
CN103641808B (zh) 2016-04-20
AU2006275587B2 (en) 2012-09-13
CN101535286A (zh) 2009-09-16
CA2617665C (en) 2014-12-02

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Granted publication date: 20140507

Termination date: 20200801