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Volumn 9, Issue 6, 1998, Pages 907-910

Enantioselective synthesis of 2-hydroxy-1-indanone, a key precursor of enantiomerically pure 1-amino-2-indanol

Author keywords

[No Author keywords available]

Indexed keywords

1 AMINO 2 INDANOL DERIVATIVE; DEXTRO PHENYLALANINE; INDANONE DERIVATIVE; INDINAVIR; ORGANIC SOLVENT; PROTEINASE INHIBITOR; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG;

EID: 0032571583     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(98)00050-0     Document Type: Article
Times cited : (34)

References (28)
  • 11
    • 0344649631 scopus 로고
    • and references cited therein
    • (b) Idem, J. Med. Chem. 1994, 37, 3443-3451, and references cited therein.
    • (1994) J. Med. Chem. , vol.37 , pp. 3443-3451
    • Idem1
  • 13
    • 0344649629 scopus 로고    scopus 로고
    • JP Patent 95-242614
    • Optically active oc-hydroxyketone 5 is reportedly available by asymmetric synthesis: Oda, Y.; Yuasa, M. JP Patent 95-242614; Chem. Abstr. 124: 55593.
    • Chem. Abstr. 124 , pp. 55593
    • Oda, Y.1    Yuasa, M.2
  • 21
    • 0345080374 scopus 로고    scopus 로고
    • note
    • Following lipases other than those listed on the Table 1 presented E>15: Fluka 62291 (Rhizomucor miehei), 21; Fluka 62293 (Thermus aquaticus), 31; Fluka 62302 (Candida cylindracea), 15; Fluka 62298 (Mucor miehei), 15.
  • 24
    • 0344218159 scopus 로고    scopus 로고
    • note
    • The c and E values obtained in the transesterification reaction of racemic 7 with an alcohol were as follows: 2-butanol, c=0.19, E=41; 9-fluorenylmethanol, c=0.43, E=1.6.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.