Chemistry of pyrrocorphins: synthesis of isobacteriochlorins and pyrrocorphins bearing a methyl group at the meso position between rings A and D


Autoria(s): Hilpert, Kurt; Leumann, Christian; Davis, Anthony P.; Eschenmoser, Albert
Data(s)

1983

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