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Volumn 99, Issue 6, 1977, Pages 1871-1880

Intramolecular Dipolar Cycloaddition Reactions of Unsaturated 2H-Azirines

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EID: 0000685044     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja00448a031     Document Type: Article
Times cited : (54)

References (89)
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    • For a recent review on Intramolecular 1,3-Dipolar Cycloadditions, see A. Padwa, Angew. Chem., Int. Ed. Engl., 15, 123 (1976).
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    • For a review of the photochemistry of 2H-azirines see
    • For a review of the photochemistry of 2H-azirines see A. Padwa, Acc. Chem. Res., 9, 371 (1976).
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    • Previous work in our laboratory has shown that the relative reactivities of nitrile ylides generated from different 2H-azirine precursors are very similar toward a given dipolarophile, thereby justifying this assumption, see
    • Previous work in our laboratory has shown that the relative reactivities of nitrile ylides generated from different 2H-azirine precursors are very similar toward a given dipolarophile, thereby justifying this assumption, see A. Padwa, J. Smolanoff, and A. I. Tremper, J. Am. Chem. Soc., 97, 4682, (1975).
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 4682
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    • For recent examples where C-C bond cleavage of a 2H-azirine occurs thermally, see
    • For recent examples where C-C bond cleavage of a 2H-azirine occurs thermally, see L. A. Wendling and R. G. Bergman, J. Am. Chem. Soc., 96, 308 (1974);
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