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Volumn 39, Issue 38, 1998, Pages 6979-6982

Synthesis of trans-fused [5,5] bicyclic lactones/lactams as templates for serine protease inhibition

Author keywords

[No Author keywords available]

Indexed keywords

CHYMOTRYPSIN; FUSED HETEROCYCLIC RINGS; LACTAM; LACTAM DERIVATIVE; LACTONE; LACTONE DERIVATIVE; LEUKOCYTE ELASTASE; REAGENT; SERINE PROTEINASE INHIBITOR;

EID: 0032541734     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01481-6     Document Type: Article
Times cited : (17)

References (17)
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    • 3. Fukazawa, S.; Iida, M.; Nakanishi, A.; Fujiinami, T.; Sakai, S. J. Chem. Soc., Chem Commun. 1987, 920-921; Shultz, N.; Totenberg-Kaulen, S.; Dapperheld, S.; Heyer, J.; Platen, M.; Schumader, K.; Steckhan, E. Stud. Org. Chem. (Amsterdam), (Recent Adv. Electroorg. Synth.) 1987, 30, 127-135; Tanaka, T. Bull. Chem. Soc. Jpn. 1959, 1320-1324; for natural products containing this system see Ma, K. W.; Chang, F. C.; Clardy, J. C. J. Chem. Soc., Chem. Commun. 1971, 424-425 and references therein; Marco, J. A.; Sanz-Cervera, F.; Pareja, J. M; Sancenon, F.; Valles-Xirau, J. Phytochemistry 1994, 477-485.
    • (1987) J. Chem. Soc., Chem Commun. , pp. 920-921
    • Fukazawa, S.1    Iida, M.2    Nakanishi, A.3    Fujiinami, T.4    Sakai, S.5
  • 7
    • 84953387901 scopus 로고
    • Recent Adv. Electroorg. Synth.
    • 3. Fukazawa, S.; Iida, M.; Nakanishi, A.; Fujiinami, T.; Sakai, S. J. Chem. Soc., Chem Commun. 1987, 920-921; Shultz, N.; Totenberg-Kaulen, S.; Dapperheld, S.; Heyer, J.; Platen, M.; Schumader, K.; Steckhan, E. Stud. Org. Chem. (Amsterdam), (Recent Adv. Electroorg. Synth.) 1987, 30, 127-135; Tanaka, T. Bull. Chem. Soc. Jpn. 1959, 1320-1324; for natural products containing this system see Ma, K. W.; Chang, F. C.; Clardy, J. C. J. Chem. Soc., Chem. Commun. 1971, 424-425 and references therein; Marco, J. A.; Sanz-Cervera, F.; Pareja, J. M; Sancenon, F.; Valles-Xirau, J. Phytochemistry 1994, 477-485.
    • (1987) Stud. Org. Chem. (Amsterdam) , vol.30 , pp. 127-135
    • Shultz, N.1    Totenberg-Kaulen, S.2    Dapperheld, S.3    Heyer, J.4    Platen, M.5    Schumader, K.6    Steckhan, E.7
  • 8
    • 0010304122 scopus 로고
    • 3. Fukazawa, S.; Iida, M.; Nakanishi, A.; Fujiinami, T.; Sakai, S. J. Chem. Soc., Chem Commun. 1987, 920-921; Shultz, N.; Totenberg-Kaulen, S.; Dapperheld, S.; Heyer, J.; Platen, M.; Schumader, K.; Steckhan, E. Stud. Org. Chem. (Amsterdam), (Recent Adv. Electroorg. Synth.) 1987, 30, 127-135; Tanaka, T. Bull. Chem. Soc. Jpn. 1959, 1320-1324; for natural products containing this system see Ma, K. W.; Chang, F. C.; Clardy, J. C. J. Chem. Soc., Chem. Commun. 1971, 424-425 and references therein; Marco, J. A.; Sanz-Cervera, F.; Pareja, J. M; Sancenon, F.; Valles-Xirau, J. Phytochemistry 1994, 477-485.
    • (1959) Bull. Chem. Soc. Jpn. , pp. 1320-1324
    • Tanaka, T.1
  • 9
    • 0010393367 scopus 로고
    • and references therein
    • 3. Fukazawa, S.; Iida, M.; Nakanishi, A.; Fujiinami, T.; Sakai, S. J. Chem. Soc., Chem Commun. 1987, 920-921; Shultz, N.; Totenberg-Kaulen, S.; Dapperheld, S.; Heyer, J.; Platen, M.; Schumader, K.; Steckhan, E. Stud. Org. Chem. (Amsterdam), (Recent Adv. Electroorg. Synth.) 1987, 30, 127-135; Tanaka, T. Bull. Chem. Soc. Jpn. 1959, 1320-1324; for natural products containing this system see Ma, K. W.; Chang, F. C.; Clardy, J. C. J. Chem. Soc., Chem. Commun. 1971, 424-425 and references therein; Marco, J. A.; Sanz-Cervera, F.; Pareja, J. M; Sancenon, F.; Valles-Xirau, J. Phytochemistry 1994, 477-485.
    • (1971) J. Chem. Soc., Chem. Commun. , pp. 424-425
    • Ma, K.W.1    Chang, F.C.2    Clardy, J.C.3
  • 10
    • 0010347903 scopus 로고
    • 3. Fukazawa, S.; Iida, M.; Nakanishi, A.; Fujiinami, T.; Sakai, S. J. Chem. Soc., Chem Commun. 1987, 920-921; Shultz, N.; Totenberg-Kaulen, S.; Dapperheld, S.; Heyer, J.; Platen, M.; Schumader, K.; Steckhan, E. Stud. Org. Chem. (Amsterdam), (Recent Adv. Electroorg. Synth.) 1987, 30, 127-135; Tanaka, T. Bull. Chem. Soc. Jpn. 1959, 1320-1324; for natural products containing this system see Ma, K. W.; Chang, F. C.; Clardy, J. C. J. Chem. Soc., Chem. Commun. 1971, 424-425 and references therein; Marco, J. A.; Sanz-Cervera, F.; Pareja, J. M; Sancenon, F.; Valles-Xirau, J. Phytochemistry 1994, 477-485.
    • (1994) Phytochemistry , pp. 477-485
    • Marco, J.A.1    Sanz-Cervera, F.2    Pareja, J.M.3    Sancenon, F.4    Valles-Xirau, J.5
  • 13
    • 85038538614 scopus 로고    scopus 로고
    • note
    • 2), 3.04 (1H, dt, J 12,12,6, 6a-H) and 5.81 (1H, br s, NH).
  • 14
    • 85038529104 scopus 로고    scopus 로고
    • note
    • 7. Crystal data, atomic co-ordinates, bond lengths and angles, and thermal parameters have been deposited at the Cambridge Crystallographic Data Centre.
  • 16
    • 85038533250 scopus 로고    scopus 로고
    • note
    • 3N, DMF, 74%; (ii) LDA, BnBr, -78 °C, THF, 12%; (iii) TBAF, 67%.
  • 17
    • 85038538678 scopus 로고    scopus 로고
    • manuscript in preparation
    • 10. Finch, H. manuscript in preparation.
    • Finch, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.