"The polymer-supported MacDonald-type porphyrin synthesis: Coupling of " by J. M. Montierth, A. G. Duran et al.

Faculty Publications

Title

The polymer-supported MacDonald-type porphyrin synthesis: Coupling of two dissimilar dipyrromethanes

Authors

J. M. Montierth, University of California, Davis
A. G. Duran, University of California, Davis
S. H. Leung, University of California, Davis
K. M. Smith, University of California, Davis
N. E. Schore, University of California, Davis

Document Type

Article

Publication Date

9-23-2000

Abstract

Syntheses of two completely unsymmetrical porphyrins have been achieved by MacDonald-type condensations of polymer-bound 9-formyldipyrromethanes with dissimilar solution-phase dipyrromethanes. The chemoselectivity of the process depends on the nature of the substituents at the α positions of the substrates. (C) 2000 Elsevier Science Ltd.

Publication Source (Journal or Book title)

Tetrahedron Letters

First Page

7423

Last Page

7426

Recommended Citation

Montierth, J., Duran, A., Leung, S., Smith, K., & Schore, N. (2000). The polymer-supported MacDonald-type porphyrin synthesis: Coupling of two dissimilar dipyrromethanes. Tetrahedron Letters, 41 (39), 7423-7426. https://doi.org/10.1016/S0040-4039(00)01269-7

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