Abstract
Many biologically active compounds possess 1-sulfonyl pyrrolidine structural motif. Therefore, the development of facile methods for the preparation of these compounds in optically pure form is relevant. One of the regio- and stereoselective approaches to the pyrrolidine derivatives is cycloaddition. Thus, this review article is an attempt to survey literature describing synthetic methods for the preparation of 1-sulfonyl pyrrolidine derivatives via various cycloaddition reactions.
Keywords: Pyrrolidines, sulfonylamides, cycloadditions, heterocycles, stereoselectivity, synthesis.
Graphical Abstract
Call for Papers in Thematic Issues
Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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