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Volumn 27, Issue 5, 1997, Pages 841-851

Synthesis and structure elucidation of 8-methyl- and 9-methyl-exo-2-carbomethoxy-endo-tricyclo[5.2.1.02,6]deca-3,8-dien- 5-ones

Author keywords

[No Author keywords available]

Indexed keywords

POLYCYCLIC HYDROCARBON;

EID: 0030998738     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919708004205     Document Type: Article
Times cited : (2)

References (19)
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    • Sakan, T.; Abe, K. Tetrahedron Lett. 1968, 2471. Tsunodo, T.; Kodama, M.; Ito, S. Tetrahedron Lett. 1983, 24, 83. Shuda, P. F.; Phillips, J. L.; Morgan, T. M. J. Org. Chem. 1986, 51, 2742. Grieco, P. A.; Abood, N. J. Org. Chem. 1989, 54, 6008. Suri, S. C. Tetrahedron Lett. 1993, 34, 8321. Mehta, G.; Praveen, M. J. Chem. Soc. Chem. Comm. 1993, 1573. Liu, Z-Y; Dong, H.; Chu, X. J. Tetrahedron 1994, 50, 12337. Mehta, G.; Praveen, M. J. Org. Chem. 1995, 60, 279. Zhu, J.; Yang, J-Y.; Klunder, A. J. H., Liu, Z-Y.; Zwanenberg, B. Tetrahedron 1995, 51, 5847 and reference 7 therein.
    • (1994) Tetrahedron , vol.50 , pp. 12337
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    • Sakan, T.; Abe, K. Tetrahedron Lett. 1968, 2471. Tsunodo, T.; Kodama, M.; Ito, S. Tetrahedron Lett. 1983, 24, 83. Shuda, P. F.; Phillips, J. L.; Morgan, T. M. J. Org. Chem. 1986, 51, 2742. Grieco, P. A.; Abood, N. J. Org. Chem. 1989, 54, 6008. Suri, S. C. Tetrahedron Lett. 1993, 34, 8321. Mehta, G.; Praveen, M. J. Chem. Soc. Chem. Comm. 1993, 1573. Liu, Z-Y; Dong, H.; Chu, X. J. Tetrahedron 1994, 50, 12337. Mehta, G.; Praveen, M. J. Org. Chem. 1995, 60, 279. Zhu, J.; Yang, J-Y.; Klunder, A. J. H., Liu, Z-Y.; Zwanenberg, B. Tetrahedron 1995, 51, 5847 and reference 7 therein.
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    • and reference 7 therein
    • Sakan, T.; Abe, K. Tetrahedron Lett. 1968, 2471. Tsunodo, T.; Kodama, M.; Ito, S. Tetrahedron Lett. 1983, 24, 83. Shuda, P. F.; Phillips, J. L.; Morgan, T. M. J. Org. Chem. 1986, 51, 2742. Grieco, P. A.; Abood, N. J. Org. Chem. 1989, 54, 6008. Suri, S. C. Tetrahedron Lett. 1993, 34, 8321. Mehta, G.; Praveen, M. J. Chem. Soc. Chem. Comm. 1993, 1573. Liu, Z-Y; Dong, H.; Chu, X. J. Tetrahedron 1994, 50, 12337. Mehta, G.; Praveen, M. J. Org. Chem. 1995, 60, 279. Zhu, J.; Yang, J-Y.; Klunder, A. J. H., Liu, Z-Y.; Zwanenberg, B. Tetrahedron 1995, 51, 5847 and reference 7 therein.
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  • 15
    • 84920296328 scopus 로고    scopus 로고
    • A large quantity of a mixture of 2 & 3 was left from different batches after partially crystallizing out 2. Further efforts to crystalize pure 2 or 3 were in vain. The computation of yield was irrelevant in this experiment
    • A large quantity of a mixture of 2 & 3 was left from different batches after partially crystallizing out 2. Further efforts to crystalize pure 2 or 3 were in vain. The computation of yield was irrelevant in this experiment.
  • 19
    • 0030004524 scopus 로고    scopus 로고
    • In this reference, the stereochemistry of carbomethoxy group in structure 4 & 5 is endo and has been corrected. Consequently, the relative stereochemistry of two carbomethoxy groups in 6 & 7 is trans.
    • Suri, S. C. Tetrahedron Lett. 1996, 37, 2335. In this reference, the stereochemistry of carbomethoxy group in structure 4 & 5 is endo and has been corrected. Consequently, the relative stereochemistry of two carbomethoxy groups in 6 & 7 is trans.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 2335
    • Suri, S.C.1


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