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Volumn 7, Issue 9, 1999, Pages 2105-2114

Design and synthesis of a novel series of HIV-1 protease inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

3 AMINO 2 HYDROXY 4 PHENYLBUTYRIC ACID; 4 [ACETYL (1 TERT BUTYLCARBAMOYL 2 PHENYLETHYL)AMINO] 1 BENZYL 2 HYDROXYBUTYL] 3 HYDROXY 2 METHYLBENZAMIDE; [4 [ACETYL (1 TERT BUTYLCARBAMOYL 2 PHENYLETHYL)AMINO] 1 BETA NAPTHYLMETHYL 2 HYDROXYBUTYL] 3 HYDROXY 2 METHYLBENZAMIDE; ANTIVIRUS AGENT; INDINAVIR; NELFINAVIR; RITONAVIR; SAQUINAVIR; UNCLASSIFIED DRUG;

EID: 0032867633     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(99)00163-7     Document Type: Article
Times cited : (5)

References (42)
  • 4
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    • For excellent reviews on HIV-1 protease inhibitors, see:
    • For excellent reviews on HIV-1 protease inhibitors, see: Wlodawer, A.; Erickson, J. W. Annu. Rev. Biochem. 1993, 62, 543.
    • (1993) Annu. Rev. Biochem. , vol.62 , pp. 543
    • Wlodawer, A.1    Erickson, J.W.2
  • 24
    • 0027488072 scopus 로고
    • For the reduction of α-amino ketones, see: and references cited therein
    • For the reduction of α-amino ketones, see: Dondoni, A., Perrone, D. Synthesis 1993, 1162 and references cited therein.
    • (1993) Synthesis , pp. 1162
    • Dondoni, A.1    Perrone, D.2
  • 25
    • 0000012858 scopus 로고
    • For the assignment of the absolute stereochemistry based on the vicinal coupling, see:
    • For the assignment of the absolute stereochemistry based on the vicinal coupling, see: Futagawa, S.; Inui, T.; Shiba, T. Bull. Chem. Soc. Jpn. 1973, 46, 3308.
    • (1973) Bull. Chem. Soc. Jpn. , vol.46 , pp. 3308
    • Futagawa, S.1    Inui, T.2    Shiba, T.3
  • 33
    • 0031013195 scopus 로고    scopus 로고
    • For the chemistry of hydroxyethylamine, see: and references cited therein
    • For the chemistry of hydroxyethylamine, see: Shiabata, N.; Katoh, T.; Terashima, S. Tetrahedron Lett. 1997, 38, 619 and references cited therein.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 619
    • Shiabata, N.1    Katoh, T.2    Terashima, S.3
  • 34
    • 0028362882 scopus 로고    scopus 로고
    • reported that o-methyl-N-methylbenzamide exhibited a preference for an orientation in which the amide carbonyl and benzene ring were not coplanar
    • Kaldor et al. reported that o-methyl-N-methylbenzamide exhibited a preference for an orientation in which the amide carbonyl and benzene ring were not coplanar. In this case, the ortho-methyl group might affected the conformation of sulfonamide, see: Kaldor, S. W.; Hammond, M.; Dressmen, B. A.; Fritz, J. E.; Crowell, T. A.; Hermann, R. A. Bioorg. Med. Chem. Lett. 1994, 4, 1385.
    • Kaldor1
  • 35
    • 0028362882 scopus 로고    scopus 로고
    • In this case, the ortho-methyl group might affected the conformation of sulfonamide, see:
    • Kaldor et al. reported that o-methyl-N-methylbenzamide exhibited a preference for an orientation in which the amide carbonyl and benzene ring were not coplanar. In this case, the ortho-methyl group might affected the conformation of sulfonamide, see: Kaldor, S. W.; Hammond, M.; Dressmen, B. A.; Fritz, J. E.; Crowell, T. A.; Hermann, R. A. Bioorg. Med. Chem. Lett. 1994, 4, 1385.
    • (1994) Bioorg. Med. Chem. Lett. , vol.4 , pp. 1385
    • Kaldor, S.W.1    Hammond, M.2    Dressmen, B.A.3    Fritz, J.E.4    Crowell, T.A.5    Hermann, R.A.6
  • 36
    • 0345231018 scopus 로고    scopus 로고
    • For the conformation of N,N-dialkyl-benzenesulfonamides, see: 29 and references cited therein
    • For the conformation of N,N-dialkyl-benzenesulfonamides, see: 29 and references cited therein.
  • 42
    • 0345231012 scopus 로고    scopus 로고
    • Compounds 19, 21, 23, 27, 32, 33, 34, 35 and 36 could not be separated by PTLC. They were assayed as diastereomixtures
    • Compounds 19, 21, 23, 27, 32, 33, 34, 35 and 36 could not be separated by PTLC. They were assayed as diastereomixtures.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.