JP2002510699A5 - - Google Patents

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Publication number
JP2002510699A5
JP2002510699A5 JP2000542335A JP2000542335A JP2002510699A5 JP 2002510699 A5 JP2002510699 A5 JP 2002510699A5 JP 2000542335 A JP2000542335 A JP 2000542335A JP 2000542335 A JP2000542335 A JP 2000542335A JP 2002510699 A5 JP2002510699 A5 JP 2002510699A5
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JP
Japan
Prior art keywords
group
formula
amine
acid
diaminocyclohexane
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.)
Granted
Application number
JP2000542335A
Other languages
English (en)
Japanese (ja)
Other versions
JP2002510699A (ja
JP4409089B2 (ja
Filing date
Publication date
Priority claimed from GBGB9807104.6A external-priority patent/GB9807104D0/en
Application filed filed Critical
Publication of JP2002510699A publication Critical patent/JP2002510699A/ja
Publication of JP2002510699A5 publication Critical patent/JP2002510699A5/ja
Application granted granted Critical
Publication of JP4409089B2 publication Critical patent/JP4409089B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2000542335A 1998-04-02 1999-04-01 ホスフィンリガンドの調製 Expired - Fee Related JP4409089B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB9807104.6 1998-04-02
GBGB9807104.6A GB9807104D0 (en) 1998-04-02 1998-04-02 The preparation of phosphine ligands
PCT/GB1999/001016 WO1999051614A1 (en) 1998-04-02 1999-04-01 Preparation of phosphine ligands

Publications (3)

Publication Number Publication Date
JP2002510699A JP2002510699A (ja) 2002-04-09
JP2002510699A5 true JP2002510699A5 (enExample) 2006-05-25
JP4409089B2 JP4409089B2 (ja) 2010-02-03

Family

ID=10829754

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2000542335A Expired - Fee Related JP4409089B2 (ja) 1998-04-02 1999-04-01 ホスフィンリガンドの調製

Country Status (10)

Country Link
US (1) US6486347B2 (enExample)
EP (1) EP1066298B1 (enExample)
JP (1) JP4409089B2 (enExample)
AT (1) ATE222258T1 (enExample)
AU (1) AU3161899A (enExample)
CA (1) CA2326113C (enExample)
DE (1) DE69902521T2 (enExample)
ES (1) ES2179634T3 (enExample)
GB (1) GB9807104D0 (enExample)
WO (1) WO1999051614A1 (enExample)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003000657A1 (en) * 2001-06-20 2003-01-03 Daiichi Pharmaceutical Co., Ltd. Diamine derivatives
JP4331595B2 (ja) * 2001-08-09 2009-09-16 第一三共株式会社 ジアミン誘導体
US20050074520A1 (en) * 2003-10-01 2005-04-07 Sensient Flavors Inc. Method for the production of natural botanical extracts
WO2007065292A1 (en) * 2005-12-05 2007-06-14 Chengdu Institute Of Biology, Chinese Academy Of Sciences Optically pure diamides and the preparation and uses thereof
CN101481388B (zh) * 2008-12-12 2011-02-23 信诺美(北京)化工科技有限公司 O-二苯基膦苯甲酸的合成方法
JP5212740B2 (ja) * 2009-10-29 2013-06-19 東レ・ファインケミカル株式会社 1,2−ジアミノシクロヘキサンの製造法
CN102936264B (zh) * 2012-11-01 2015-02-18 北京百灵威科技有限公司 一种芳香基手性噁唑啉膦配体的合成方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE793107A (nl) 1972-01-13 1973-06-21 Shell Int Research Werkwijze ter bereiding van ortho-dihydrocarbylfosfinobenzoezuren
WO1993012260A2 (en) * 1991-12-09 1993-06-24 Board Of Trustees Of The Leland Stanford Junio Asymmetric ligands useful for transition metal catalyzed bond forming reactions
US5739396A (en) 1991-12-09 1998-04-14 Stanford University Asymmetric ligands useful for transition metal catalyzed bond forming reactions
US5399771A (en) 1994-06-01 1995-03-21 Merck & Co., Inc. Process of synthesizing binaphthyl derivatives
DE19620023C2 (de) * 1996-05-17 2001-03-08 Celanese Chem Europe Gmbh Verfahren zur Herstellung von Phosphinat- oder Phosphonatgruppen enthaltenden tertiären Phosphanen und neue Phosphinatgruppen enthaltende tertiäre Phosphane
US6140265A (en) 1995-07-25 2000-10-31 Clariant Gmbh Catalyst for cross-coupling reactions

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