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- W2000892715 abstract "A collection of 33 hydrodipyrrins (9 targets, 21 intermediates, and 3 byproducts) has been prepared. The hydrodipyrrins (dihydrodipyrrins, tetrahydrodipyrrins, and hexahydrodipyrrins) contain a pyrrole ring and a geminal-dimethyl substituted 1-pyrroline (or pyrrolidine) ring. The α-substituents on the pyrrole ring (H, Br, CHO) and pyrroline ring (H, CH3, CH(OR)2, OMe, SMe) provide different reactivity combinations (Nu−, E+) and 0, 1, or 2 carbon atoms (which can give rise to the bridging meso-carbons in hydroporphyrins). Straightforward access to various hydrodipyrrins should facilitate development of syntheses of diverse hydroporphyrins." @default.
- W2000892715 created "2016-06-24" @default.
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- W2000892715 creator A5083917347 @default.
- W2000892715 date "2007-01-01" @default.
- W2000892715 modified "2023-09-26" @default.
- W2000892715 title "Synthesis of hydrodipyrrins tailored for reactivity at the 1- and 9-positions" @default.
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- W2000892715 doi "https://doi.org/10.1016/j.tet.2006.10.027" @default.
- W2000892715 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1857285" @default.
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