Chemistry: molecular biology and microbiology – Process of utilizing an enzyme or micro-organism to destroy... – Resolution of optical isomers or purification of organic...
Reexamination Certificate
2006-10-03
2006-10-03
Marx, Irene (Department: 1651)
Chemistry: molecular biology and microbiology
Process of utilizing an enzyme or micro-organism to destroy...
Resolution of optical isomers or purification of organic...
C435S108000, C435S170000, C435S171000, C435S169000
Reexamination Certificate
active
07115412
ABSTRACT:
Disclosed are a process for preparation of an optically active 7-substituted 3-(2-aminopropyl)indole compound and an intermediate therefor. In the above preparation process, 7-substituted indole is reacted with L- or DL-serine in the presence of a tryptophan-synthesizing enzyme originating in microorganisms to form corresponding 7-substituted L-tryptophan, and it is subjected, if necessary, to reduction, protection, exchange and elimination.
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K. Helen Ekborg Ott, et al., “Highly Enantioselective HPLC Separations Using the Covalently Bonded Macrocyclic Antibiotic, Ristocetin A, Chiral Stationary Phase”, Chirality, vol. 10, No. 5, pp. 434 to 483, 1998.
Jhon C. Gebler et al., “Dimethylallyltryptophan Synthase. An Enzyme-Catalyzed Electrophilic Aromatic Substitution”, J. Am. Chem. Soc., vol. 114, No. 19, pp. 7354-7360, 1992.
E.M.M. Van Den Berg et al., “Chemo-enzymic synthesis and characterization of L-tryptophan selectively 13C-enriched or hydroxylated in the six-membered ring using transformedEscherichia colicells”, Recueil Des Travaux Chimiques Des Pays-Bas, 109(4), pp. 287-297, XP002082902, 1990.
Fujii Akihito
Harada Hiroshi
Hirose Yoichiro
Kato Shiro
Narita Takao
Dainippon Pharmaceutical Co., Ltd.
Marx Irene
Mercian Corporation
Wenderoth , Lind & Ponack, L.L.P.
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