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Issue 5, 1993
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exo-Selective acceleration of an intermolecular Diels–Alder reaction by a trimeric porphyrin host

Abstract

A bimolecular Diels–Alder reaction is accelerated substantially and stereoselectively by binding diene and dienophile within the cavity of a cyclic metalloporphyrin trimer.

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Article type: Paper
DOI: 10.1039/C39930000458
Citation: J. Chem. Soc., Chem. Commun., 1993,0, 458-460
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    exo-Selective acceleration of an intermolecular Diels–Alder reaction by a trimeric porphyrin host

    C. J. Walter, H. L. Anderson and J. K. M. Sanders, J. Chem. Soc., Chem. Commun., 1993, 0, 458
    DOI: 10.1039/C39930000458

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