메뉴 건너뛰기




Volumn 38, Issue 34, 1997, Pages 5913-5916

Preparation of novel tricyclic diazo carbapenems: Application of inverse electron demand Diels-Alder reactions of 3,6-bis(methylthio)-1,2,4,5-tetrazine

Author keywords

[No Author keywords available]

Indexed keywords

CARBAPENEM DERIVATIVE;

EID: 0030738040     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)01321-X     Document Type: Article
Times cited : (25)

References (19)
  • 3
    • 0028265575 scopus 로고
    • Perboni, A.; Tamburini, B.; Rossi, T.; Donati, D.; Tarzia, G.; Gaviraghi, G. in "Recent Advances in the Chemistry of Anti-infective Agents"-Eds. Bently, P. H.; Ponsford, R., RSC Cambridge, pp 21-35, 1992. Padova, A.; Roberts, S. M; Donati, D.; Perboni, A.; Rossi, T., J. Chem. Soc. Chem. Commun. 1994, 441. Andreotti, D.; Rossi, T.; Marchioro, C. Biorg. Med Chem. Lett. 1996, 6, 2589.
    • (1994) J. Chem. Soc. Chem. Commun. , pp. 441
    • Padova, A.1    Roberts, S.M.2    Donati, D.3    Perboni, A.4    Rossi, T.5
  • 4
    • 0030571299 scopus 로고    scopus 로고
    • Perboni, A.; Tamburini, B.; Rossi, T.; Donati, D.; Tarzia, G.; Gaviraghi, G. in "Recent Advances in the Chemistry of Anti-infective Agents"-Eds. Bently, P. H.; Ponsford, R., RSC Cambridge, pp 21-35, 1992. Padova, A.; Roberts, S. M; Donati, D.; Perboni, A.; Rossi, T., J. Chem. Soc. Chem. Commun. 1994, 441. Andreotti, D.; Rossi, T.; Marchioro, C. Biorg. Med Chem. Lett. 1996, 6, 2589.
    • (1996) Biorg. Med Chem. Lett. , vol.6 , pp. 2589
    • Andreotti, D.1    Rossi, T.2    Marchioro, C.3
  • 6
    • 0029822636 scopus 로고    scopus 로고
    • Hannesian, S.; Rozema, M. J.; Reddy, G. B.; and Braganza, J. F. Biorg. Med. Chem. Lett. 1995, 5, 2525. Alcaide, B.; Polanco, C.; Saez, E.; Sierra, M. A. J. Org. Chem. 1996, 61, 7125.
    • (1996) J. Org. Chem. , vol.61 , pp. 7125
    • Alcaide, B.1    Polanco, C.2    Saez, E.3    Sierra, M.A.4
  • 8
    • 0003719612 scopus 로고
    • Academic Press: San Diego
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis, Academic Press: San Diego,1987; Boger, D. L.; Patel, M. Progress in Heterocyclic Chemistry, Vol. 1; Suschizky, H.; Scriven, E. F. V., Eds.; Pergamon Press: London, 1989, p 30; Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149; Boger, D. L. Chem. Rev. 1986, 86, 781.
    • (1987) Hetero Diels-alder Methodology in Organic Synthesis
    • Boger, D.L.1    Weinreb, S.M.2
  • 9
    • 85012738894 scopus 로고
    • Suschizky, H.; Scriven, E. F. V., Eds.; Pergamon Press: London
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis, Academic Press: San Diego,1987; Boger, D. L.; Patel, M. Progress in Heterocyclic Chemistry, Vol. 1; Suschizky, H.; Scriven, E. F. V., Eds.; Pergamon Press: London, 1989, p 30; Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149; Boger, D. L. Chem. Rev. 1986, 86, 781.
    • (1989) Progress in Heterocyclic Chemistry , vol.1 , pp. 30
    • Boger, D.L.1    Patel, M.2
  • 10
    • 0000229010 scopus 로고    scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis, Academic Press: San Diego,1987; Boger, D. L.; Patel, M. Progress in Heterocyclic Chemistry, Vol. 1; Suschizky, H.; Scriven, E. F. V., Eds.; Pergamon Press: London, 1989, p 30; Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149; Boger, D. L. Chem. Rev. 1986, 86, 781.
    • (1996) Chemtracts: Org. Chem. , vol.9 , pp. 149
    • Boger, D.L.1
  • 11
    • 33845376451 scopus 로고
    • Boger, D. L.; Weinreb, S. M. Hetero Diels-Alder Methodology in Organic Synthesis, Academic Press: San Diego,1987; Boger, D. L.; Patel, M. Progress in Heterocyclic Chemistry, Vol. 1; Suschizky, H.; Scriven, E. F. V., Eds.; Pergamon Press: London, 1989, p 30; Boger, D. L. Chemtracts: Org. Chem. 1996, 9, 149; Boger, D. L. Chem. Rev. 1986, 86, 781.
    • (1986) Chem. Rev. , vol.86 , pp. 781
    • Boger, D.L.1
  • 12
    • 33845280522 scopus 로고
    • Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415; Boger, D. L.; Zhang, M. J. J. Am. Chem. Soc. 1991,113, 4230; Panek, J. S. and Zhu, B. Tetrahedron Lett. 1996, 37, 8151.
    • (1988) J. Org. Chem. , vol.53 , pp. 1415
    • Boger, D.L.1    Sakya, S.M.2
  • 13
    • 0025871436 scopus 로고
    • Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415; Boger, D. L.; Zhang, M. J. J. Am. Chem. Soc. 1991,113, 4230; Panek, J. S. and Zhu, B. Tetrahedron Lett. 1996, 37, 8151.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4230
    • Boger, D.L.1    Zhang, M.J.2
  • 14
    • 0030569267 scopus 로고    scopus 로고
    • Boger, D. L.; Sakya, S. M. J. Org. Chem. 1988, 53, 1415; Boger, D. L.; Zhang, M. J. J. Am. Chem. Soc. 1991,113, 4230; Panek, J. S. and Zhu, B. Tetrahedron Lett. 1996, 37, 8151.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 8151
    • Panek, J.S.1    Zhu, B.2
  • 17
    • 0027321591 scopus 로고
    • Iwata-Reuyl, D.; Basak, A.; Silverman, L. S.; Engle, C. A.; Townsend, C. A. J. Nat. Prod., 1993, 56, 1373-96. Attempted preparation of the unprotected alkynyl azetidinone in an analogous manner to that used for the vinyl case (alkynylmagnesium bromide, -78 °C - it) resulted only in the dimerization of the phenyl sulfonyl azetidinone 6.
    • (1993) J. Nat. Prod. , vol.56 , pp. 1373-1396
    • Iwata-Reuyl, D.1    Basak, A.2    Silverman, L.S.3    Engle, C.A.4    Townsend, C.A.5
  • 19
    • 0342478972 scopus 로고    scopus 로고
    • All the compounds were characterized by NMR, IR, and MS and are consistent with the structures
    • All the compounds were characterized by NMR, IR, and MS and are consistent with the structures.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.