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Journal ArticleDOI

Allyl sulfones as synthons for 1,1- and 1,3-dipoles via organopalladium chemistry

Barry M. Trost, +2 more
- 01 Aug 1980 - 
- Vol. 102, Iss: 18, pp 5979-5981
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This article is published in Journal of the American Chemical Society.The article was published on 1980-08-01. It has received 122 citations till now. The article focuses on the topics: Organopalladium.

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Selectivity in palladium catalysed allylic substitution

TL;DR: Palladium catalysed allylic substitution has emerged as one of the more useful synthetic methods for the construction of C-C and C-X bonds as mentioned in this paper, which offers the advantages of mild reaction conditions, as well as the ability to accomodate a wide range of nucleophiles and their electrophilic partners.
Journal ArticleDOI

Evolving organic synthesis fostered by the pluripotent phenylsulfone moiety.

TL;DR: A comprehensive program for the synthesis of natural (or unnatural) products is analogous to the construction of a pyramid, where careful planning followed by installation of numerous levels of support are required to complete the edifice.
Journal ArticleDOI

Chemical Chameleons. Organosulfones as Synthetic Building Blocks

TL;DR: An overview of the duality of function of organosulfones as nucleophiles in basic media and electrophiles in Lewis acidic media, a change of reactivity for which they have been dubbed "chemical chameleons" is presented in this article.
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