Chemistry of pyrrocorphins: synthesis of isobacteriochlorins and pyrrocorphins bearing a methyl group at the meso position between rings A and D
Data(s) |
1983
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Resumo |
A sigmatropic methyl shift from the angular position C-1 in ring to the position C-20 between rings and constitutes the crucial step in syntheses leading to a 20-methyl-isobacteriochlorin and to 20-methyl-pyrrocorphins which served as substrates in the investigation presented in the accompanying communication. |
Formato |
application/pdf |
Identificador |
http://boris.unibe.ch/68884/1/c39830001401.pdf Hilpert, Kurt; Leumann, Christian; Davis, Anthony P.; Eschenmoser, Albert (1983). Chemistry of pyrrocorphins: synthesis of isobacteriochlorins and pyrrocorphins bearing a methyl group at the meso position between rings A and D. Journal of the Chemical Society, Chemical Communications(23), p. 1401. Royal Society of Chemistry 10.1039/c39830001401 <http://dx.doi.org/10.1039/c39830001401> doi:10.7892/boris.68884 info:doi:10.1039/c39830001401 urn:issn:0022-4936 |
Idioma(s) |
eng |
Publicador |
Royal Society of Chemistry |
Relação |
http://boris.unibe.ch/68884/ |
Direitos |
info:eu-repo/semantics/restrictedAccess |
Fonte |
Hilpert, Kurt; Leumann, Christian; Davis, Anthony P.; Eschenmoser, Albert (1983). Chemistry of pyrrocorphins: synthesis of isobacteriochlorins and pyrrocorphins bearing a methyl group at the meso position between rings A and D. Journal of the Chemical Society, Chemical Communications(23), p. 1401. Royal Society of Chemistry 10.1039/c39830001401 <http://dx.doi.org/10.1039/c39830001401> |
Palavras-Chave | #570 Life sciences; biology #540 Chemistry |
Tipo |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion PeerReviewed |