메뉴 건너뛰기




Volumn 6, Issue 17, 1996, Pages 2053-2058

Synthesis of constrained thiorphan analogs as inhibitors of neutral endopeptidase

Author keywords

[No Author keywords available]

Indexed keywords

ENZYME INHIBITOR; MEMBRANE METALLOENDOPEPTIDASE; THIORPHAN; THIORPHAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0030567870     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0960-894X(96)00367-8     Document Type: Article
Times cited : (5)

References (25)
  • 11
    • 85030271844 scopus 로고    scopus 로고
    • World Patent WO 91/09840
    • (a) Neustadt, B. World Patent WO 91/09840.
    • Neustadt, B.1
  • 12
    • 85030275150 scopus 로고    scopus 로고
    • US Patent 5, 252, 601, 1993
    • (b) Flynn G. A.; Beight, D. W.; US Patent 5, 252, 601, 1993.
    • Flynn, G.A.1    Beight, D.W.2
  • 15
    • 0000969622 scopus 로고
    • Turchaninova, L.P.; Voronkov, M. G.; Shipov, A. G.; Korchevin, N. A.; Baukov, Y. I.; Deryagina, E. N. Zh. Obshch. Khim. 1989, 59, 722. Experimental procedure for preparation of chloromethyl sulfides: To a mixture of 15.9 mL (125 mmol) TMSCl and 1.5 g (50 mmol) paraformaldehyde at 0 °C was added 7.0 mL (50 mmol) para-methoxybenzyl mercaptan. The mixture was stirred 2 h while warming to 20 °C, then distilled, bp 90-96 °C/0.1 torr. Yield: 3.5 g (34%).
    • (1989) Zh. Obshch. Khim. , vol.59 , pp. 722
    • Turchaninova, L.P.1    Voronkov, M.G.2    Shipov, A.G.3    Korchevin, N.A.4    Baukov, Y.I.5    Deryagina, E.N.6
  • 17
    • 85030274056 scopus 로고    scopus 로고
    • See ref 10. bp 80-86 °C/75 torr. Yield: 60%
    • See ref 10. bp 80-86 °C/75 torr. Yield: 60%.
  • 21
    • 33646274424 scopus 로고
    • Baumgarten, H. E., Ed.; Wiley: New York
    • For the preparation of 6e see: (a) Pearlman W. M. Org. Synth. Collect. Vol. 5; Baumgarten, H. E., Ed.; Wiley: New York, 1973; p 760.
    • (1973) Org. Synth. Collect. , vol.5 , pp. 760
    • Pearlman, W.M.1
  • 24
    • 85030279548 scopus 로고    scopus 로고
    • The enantiomers of 1b were separated on a cyclodextrin column. The (+) enantiomer eluted first and was purified to ∼96% ee. The (-) enantiomer was purified to ∼86% ee
    • The enantiomers of 1b were separated on a cyclodextrin column. The (+) enantiomer eluted first and was purified to ∼96% ee. The (-) enantiomer was purified to ∼86% ee.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.