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Volumn 52, Issue 9, 1996, Pages 3247-3260

Studies on the intramolecular cycloaddition reaction of isomünchnones derived from N-alkenyl substituted diazoimides

Author keywords

[No Author keywords available]

Indexed keywords

BENZAMIDE DERIVATIVE;

EID: 0030021791     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(95)01108-0     Document Type: Article
Times cited : (29)

References (39)
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    • (1992) Tetrahedron Lett. , vol.33 , pp. 4731
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    • Padwa, A.; Hertzog, D. L.; Chinn, R. L. Tetrahedron Lett. 1989, 30, 4077. Doyle, M. P.; Pieters, R. J.; Taunton, J.; Pho, H. Q.; Padwa, A.; Hertzog, D. L.; Precedo, L. J. Org. Chem. 1991, 56, 820. Hertzog, D. L.; Austin, D. J.; Nadler, W. R.; Padwa, A. Tetrahedron Lett. 1992, 33, 4731. Padwa, A.; Hertzog, D. L. Tetrahedron 1993, 49, 2589.
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    • We thank Professor Kosta Steliou of Boston University for providing a copy of the extensively rewritten Still Model program and for providing a VMS version of MMX
    • We thank Professor Kosta Steliou of Boston University for providing a copy of the extensively rewritten Still Model program and for providing a VMS version of MMX.
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    • note
    • The results obtained with 26 show that there must be reversible formation of the 1,3-dipole, since in the absence of the dipolarophile, the non 1,3-dipole products are formed in 77% yield, whereas in the presence of N-phenyl maleimide, a 60-100% yield of the 1,3-dipolar cycloadduct is formed.


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