Diastereodirected Alkylation of Ketones and 1,3-Diketones with N-[1H-Indol-3-yl(phenyl)methyl]-N-methylamine by the Michael Reaction View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2005-06

AUTHORS

B. B. Semenov, Yu. I. Smushkevich, I. I. Levina, L. N. Kurkovskaya, K. A. Lysenko, V. V. Kachala

ABSTRACT

A method has been developed for introducing the 1H-indol-3-yl(phenyl)methyl residue into position 2 of ketones and 1,3-diketones. The principle of bringing in controlled diastereoselectivity based on the configuration of intermediates is demonstrated.

PAGES

730-738

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s10593-005-0213-5

DOI

http://dx.doi.org/10.1007/s10593-005-0213-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1009984437


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