ES2166930T3 - Nuevo procedimiento eficaz y altamente selectivo para enantiomeros para la preparacion de beta-aminoacidos de ciclorentano enantiomericamente puros. - Google Patents

Nuevo procedimiento eficaz y altamente selectivo para enantiomeros para la preparacion de beta-aminoacidos de ciclorentano enantiomericamente puros.

Info

Publication number
ES2166930T3
ES2166930T3 ES97106550T ES97106550T ES2166930T3 ES 2166930 T3 ES2166930 T3 ES 2166930T3 ES 97106550 T ES97106550 T ES 97106550T ES 97106550 T ES97106550 T ES 97106550T ES 2166930 T3 ES2166930 T3 ES 2166930T3
Authority
ES
Spain
Prior art keywords
preparation
enantiomerically pure
cyclorentane
enantiomers
beta
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 - Lifetime
Application number
ES97106550T
Other languages
English (en)
Inventor
Joachim Dr Mittendorf
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.)
Bayer AG
Original Assignee
Bayer AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Application granted granted Critical
Publication of ES2166930T3 publication Critical patent/ES2166930T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/30Preparation of optical isomers
    • C07C227/32Preparation of optical isomers by stereospecific synthesis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/24Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a ring other than a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/74Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08Systems containing only non-condensed rings with a five-membered ring the ring being saturated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

EL METODO DE LA INVENCION PARA LA PREPARACION DE CICLOPENTAN {BE} ERAL (I) DONDE A Y D TIENEN LOS SIGNIFICADOS MENCIONADOS EN LA DESCRIPCION, SEGUN EL CUAL SE TRANSFORMAN ANHIDRIDOS MESO DICARBOXILICOS EN MONOESTERES DICARBOXILICOS ENANTIOMERICAMENTE PUROS MEDIANTE ALCOHOLISIS ASIMETRICA CON ALQUILALCOHOLES Y EN PRESENCIA DE UNA BASE AMINA QUIRAL EN FORMA ENANTIOMERICAMENTE PURA, EN DISOLVENTES INERTES, A TRAVES DE LA SAL INTERMEDIA ENANTIOMERICAMENTE PURA, EN UN PASO POSTERIOR DE UNA TRANSPOSICION DE CURTIUS SE TRANSFORMAN ESTOS MONOESTERES DICARBOXILICOS MEDIANTE REACCION CON UN INTERMEDIARIO AZIDA EN LAS CORRESPONDIENTES AZIDAS DE ACIDOS Y A CONTINUACION EN LOS CORRESPONDIENTES ISOCIANATOS TRANSPUESTOS, DESPUES REACCIONAN LOS ISOCIANATOS CON ALQUILALCOHOLES FORMANDO LOS COMPUESTOS DE FORMULA GENERAL (VII) Y FINALMENTE, MEDIANTE DISOCIACION DE LAS FUNCIONES URETANO Y ESTER, SE OBTIENEN LOS CICLOPENTAN FORMULA GENERAL (I).
ES97106550T 1996-05-03 1997-04-21 Nuevo procedimiento eficaz y altamente selectivo para enantiomeros para la preparacion de beta-aminoacidos de ciclorentano enantiomericamente puros. Expired - Lifetime ES2166930T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19617772A DE19617772A1 (de) 1996-05-03 1996-05-03 Neues effizientes und hochenantioselektives Verfahren zur Herstellung von enantiomerenreinen Cyclopentan-beta-aminosäuren

Publications (1)

Publication Number Publication Date
ES2166930T3 true ES2166930T3 (es) 2002-05-01

Family

ID=7793231

Family Applications (1)

Application Number Title Priority Date Filing Date
ES97106550T Expired - Lifetime ES2166930T3 (es) 1996-05-03 1997-04-21 Nuevo procedimiento eficaz y altamente selectivo para enantiomeros para la preparacion de beta-aminoacidos de ciclorentano enantiomericamente puros.

Country Status (25)

Country Link
US (1) US5877343A (es)
EP (1) EP0805145B1 (es)
JP (1) JPH1087586A (es)
KR (1) KR970074749A (es)
CN (1) CN1168883A (es)
AR (2) AR006944A1 (es)
AT (1) ATE207876T1 (es)
AU (1) AU1915697A (es)
BR (1) BR9701983A (es)
CA (1) CA2204055A1 (es)
CZ (1) CZ135397A3 (es)
DE (2) DE19617772A1 (es)
DK (1) DK0805145T3 (es)
ES (1) ES2166930T3 (es)
HR (1) HRP970214A2 (es)
HU (1) HU9700831D0 (es)
ID (1) ID16859A (es)
IL (1) IL120747A0 (es)
NO (1) NO971983L (es)
PL (1) PL319775A1 (es)
PT (1) PT805145E (es)
SI (1) SI0805145T1 (es)
SK (1) SK55497A3 (es)
SV (1) SV1997000031A (es)
ZA (1) ZA973796B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60102825T2 (de) * 2000-07-31 2005-03-31 Brandeis University, Waltham Kinetische racematspaltung chiraler 2- und 3- substituierter carbonsäuren
EP1419125A4 (en) * 2001-07-31 2005-03-23 Univ Brandeis KINETIC RACEMAT SPLITS OF CHIRALER 2 AND 3 SUBSTITUTED CARBOXYLIC ACIDS
US7531662B2 (en) * 2003-06-11 2009-05-12 Brandeis University Cinchona-alkaloid-based catalysts, and asymmetric alcoholysis of cyclic anhydrides using them

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3560565A (en) * 1969-06-03 1971-02-02 American Home Prod 1-amino-n-sulfonylcyclopentane-carboxamides
GB8716278D0 (en) * 1987-07-10 1987-08-19 Fujisawa Pharmaceutical Co Antimicrobial agent
AU673824B2 (en) * 1992-05-29 1996-11-28 Bayer Aktiengesellschaft Cyclopentane- and -pentene-beta-amino acids
DE4400749A1 (de) * 1994-01-13 1995-07-20 Bayer Ag Neues hochenantioselektives Verfahren zur Herstellung von enantiomerenreinen Cyclopentan- und -penten-beta-Aminosäuren

Also Published As

Publication number Publication date
CA2204055A1 (en) 1997-11-03
AR013071A2 (es) 2000-12-13
KR970074749A (ko) 1997-12-10
ID16859A (id) 1997-11-20
IL120747A0 (en) 1997-09-30
MX9702768A (es) 1997-11-29
CN1168883A (zh) 1997-12-31
AR006944A1 (es) 1999-09-29
ZA973796B (en) 1997-12-01
SV1997000031A (es) 1997-10-23
PT805145E (pt) 2002-03-28
EP0805145A1 (de) 1997-11-05
DE59705135D1 (de) 2001-12-06
HU9700831D0 (en) 1997-06-30
ATE207876T1 (de) 2001-11-15
AU1915697A (en) 1997-11-06
PL319775A1 (en) 1997-11-10
SK55497A3 (en) 1997-11-05
BR9701983A (pt) 1998-09-15
SI0805145T1 (en) 2002-02-28
EP0805145B1 (de) 2001-10-31
NO971983D0 (no) 1997-04-29
DE19617772A1 (de) 1997-11-13
JPH1087586A (ja) 1998-04-07
CZ135397A3 (cs) 1998-05-13
NO971983L (no) 1997-11-04
US5877343A (en) 1999-03-02
DK0805145T3 (da) 2002-03-04
HRP970214A2 (en) 1998-04-30

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