JP4301757B2 - エナンチオマー濃縮されたＮ−アシル化されたβ−アミノ酸の製造方法並びに保護基分離によるβ−アミノ酸の製造方法及びその使用 - Google Patents

エナンチオマー濃縮されたＮ−アシル化されたβ−アミノ酸の製造方法並びに保護基分離によるβ−アミノ酸の製造方法及びその使用 Download PDF

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JP4301757B2
JP4301757B2 JP2002002691A JP2002002691A JP4301757B2 JP 4301757 B2 JP4301757 B2 JP 4301757B2 JP 2002002691 A JP2002002691 A JP 2002002691A JP 2002002691 A JP2002002691 A JP 2002002691A JP 4301757 B2 JP4301757 B2 JP 4301757B2
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alkyl
acylated
hydrogenation
amino acid
cycloalkyl
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JP2002265425A (ja
JP2002265425A5 (https=
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クリマー ハンス−ペーター
ドラウツ カールハインツ
ラング ユッタ
ベルナー アルミン
ヘラー デトレフ
ホルツ イェンス
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Evonik Operations GmbH
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Evonik Degussa GmbH
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00—Preparation of carboxylic acid amides
    • C07C231/12—Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
JP2002002691A 2001-01-11 2002-01-09 エナンチオマー濃縮されたＮ−アシル化されたβ−アミノ酸の製造方法並びに保護基分離によるβ−アミノ酸の製造方法及びその使用 Expired - Fee Related JP4301757B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10100971.2 2001-01-11
DE10100971A DE10100971A1 (de) 2001-01-11 2001-01-11 Verfahren zur Herstellung enantiomerenangereicherter beta-Aminosäure

Publications (3)

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JP2002265425A JP2002265425A (ja) 2002-09-18
JP2002265425A5 JP2002265425A5 (https=) 2005-07-14
JP4301757B2 true JP4301757B2 (ja) 2009-07-22

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JP2002002691A Expired - Fee Related JP4301757B2 (ja) 2001-01-11 2002-01-09 エナンチオマー濃縮されたＮ−アシル化されたβ−アミノ酸の製造方法並びに保護基分離によるβ−アミノ酸の製造方法及びその使用

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US (1) US6492544B2 (https=)
EP (1) EP1225166B1 (https=)
JP (1) JP4301757B2 (https=)
AT (1) ATE279388T1 (https=)
DE (2) DE10100971A1 (https=)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7007861B2 (en) 2000-06-08 2006-03-07 S.C. Johnson & Son, Inc. Methods and personal protection devices for repelling insects
MXPA03004168A (es) * 2000-12-13 2004-12-02 Warner Lambert Co Sintesis de ligandos bisfosfolanos p-quirales y de sus complejos con metales de transicion para uso como catalizadores de hidrogenacion asimetrica.
JP4226847B2 (ja) * 2001-07-24 2009-02-18 高砂香料工業株式会社 ホスフィン−ホスホラン化合物と遷移金属とを含有する遷移金属錯体の存在下、α，β−不飽和アミド誘導体から光学活性アミド類を製造する方法。
GB0120167D0 (en) * 2001-08-17 2001-10-10 Chirotech Technology Ltd Asymmetric hydrogenation
WO2003042135A2 (en) * 2001-11-09 2003-05-22 The Penn State Research Foundation P-chiral phospholanes and phosphocyclic compounds and their use in asymmetric catalytic reactions
US7169953B2 (en) * 2001-11-09 2007-01-30 The Penn State Research Foundation P-chiral phospholanes and phosphocyclic compounds and their use in asymmetric catalytic reactions
CN1318433C (zh) * 2002-04-04 2007-05-30 德古萨股份公司 作为二齿配体的双膦
US7084089B2 (en) * 2002-07-31 2006-08-01 Shell Oil Company Process for the carbonylation of ethylenically unsaturated compounds, bidentate diphosphine composition used in this process and a process for preparation of this bidentate diphosphine composition
US6806391B2 (en) 2002-07-31 2004-10-19 Shell Oil Company Process for the carbonylation of ethylenically unsaturated compounds and bidentate diphosphine composition used in this process
AR043515A1 (es) * 2003-03-19 2005-08-03 Merck & Co Inc Procedimiento para preparar derivados quirales beta aminoacidos mediante hidrogenacion asimetrica
TW200602293A (en) * 2004-04-05 2006-01-16 Merck & Co Inc Process for the preparation of enantiomerically enriched beta amino acid derivatives
US7013601B2 (en) * 2004-07-22 2006-03-21 Coastal Planters, Llc Plant container with hanger
US7618410B2 (en) * 2004-10-05 2009-11-17 Cardia Access, Inc. Devices and methods for access through a tissue wall
DE102005014055A1 (de) * 2005-03-23 2006-09-28 Degussa Ag Unsymmetrisch substituierte Phospholankatalysatoren
DE102005037649A1 (de) * 2005-08-05 2007-02-08 Leibniz-Institut Für Katalyse E.V. An Der Universität Rostock Homogene katalytische Hydrierung
EP2070904A1 (en) 2007-12-12 2009-06-17 Laboratorios Del. Dr. Esteve, S.A. Rhodium-phosphorus complexes and their use in ring opening reactions
EP2070903A1 (en) 2007-12-12 2009-06-17 Laboratorios del Dr. Esteve S.A. Microwave-assisted ring opening reaction

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999059721A1 (en) * 1998-05-18 1999-11-25 The Penn State Research Foundation Catalytic asymmetric hydrogenation, hydroformylation, and hydrovinylation via transition metal catalysts with phosphines and phosphites
ATE233780T1 (de) * 1998-11-05 2003-03-15 Chirotech Technology Ltd Chirale ligande für asymmetrische katalysis

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Publication number Publication date
EP1225166A1 (de) 2002-07-24
US6492544B2 (en) 2002-12-10
DE50104095D1 (de) 2004-11-18
ATE279388T1 (de) 2004-10-15
JP2002265425A (ja) 2002-09-18
DE10100971A1 (de) 2002-07-18
US20020128509A1 (en) 2002-09-12
EP1225166B1 (de) 2004-10-13

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