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- W1494658640 endingPage "156" @default.
- W1494658640 startingPage "115" @default.
- W1494658640 abstract "Three- and four-membered carbocycles are very important entities in the field of organic chemistry. Their significant ring strain affords very interesting chemical properties as well as biological activities when these small-sized rings are present in the structure of natural products. This chapter focuses on organo- and transition-metal-catalyzed multiple bond-forming transformations (MBFTs) that have emerged as efficient strategies to construct small three- and four-membered carbocycles in high selectivities. The syntheses of four-membered carbocycles are much less described than those of three-membered ones. Because of the nature of their structures, domino approaches are clearly the methods of choice for their construction. Among them, transition-metal- and organo-catalyzed strategies are clearly the most popular ones, allowing the stereoselective construction of contiguous stereogenic centers in high selectivities, though catalytic and asymmetric approaches are mainly described using organocatalyts in Michael-Initiated Ring-Closure (MIRC) processes." @default.
- W1494658640 created "2016-06-24" @default.
- W1494658640 creator A5043172611 @default.
- W1494658640 creator A5067997838 @default.
- W1494658640 creator A5089132074 @default.
- W1494658640 date "2015-04-24" @default.
- W1494658640 modified "2023-09-27" @default.
- W1494658640 title "Three- and Four-Membered Carbocycles" @default.
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