Matches in SemOpenAlex for { <https://semopenalex.org/work/W2512679420> ?p ?o ?g. }
- W2512679420 endingPage "714" @default.
- W2512679420 startingPage "655" @default.
- W2512679420 abstract "This chapter outlines the key bond constructions and strategies that enabled the synthesis of highly complex targets. However, despite these advances, there are still opportunities for the development of improved methods and catalysts. Although some advances have been made in the enantioselective Morita-Baylis-Hillman (MBH) reaction of methyl acrylate, the original Baylis and Hillman substrate, a general solution providing access to the products with high enantiomeric selectivity over a reasonable time frame using a readily available catalyst for a wide range of aldehyde electrophiles has not been realized. Similarly, an enantioselective version of the reaction described by Morita using acrylonitrile as the substrate has also not been demonstrated. Given the significant contributions made in reaction development and the mechanistic insight garnered by detailed evaluation of the newly developed reactions, the prospects for future advances that continue the current trajectory of innovative design and applications in synthesis are good." @default.
- W2512679420 created "2016-09-16" @default.
- W2512679420 creator A5049368672 @default.
- W2512679420 creator A5081807832 @default.
- W2512679420 creator A5084800322 @default.
- W2512679420 date "2016-07-25" @default.
- W2512679420 modified "2023-10-10" @default.
- W2512679420 title "Morita-Baylis-Hillman, Vinylogous Morita-Baylis-Hillman, and Rauhut-Currier Reactions" @default.
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