Matches in SemOpenAlex for { <https://semopenalex.org/work/W2803482054> ?p ?o ?g. }
- W2803482054 endingPage "191" @default.
- W2803482054 startingPage "129" @default.
- W2803482054 abstract "Transition-metal-catalyzed carbene coupling reactions have been recently extensively explored as a new type of carbon–carbon bond-forming methodology. The carbene migratory insertion is proposed as the key step in these coupling reactions. This carbene insertion process can be incorporated with many other transformations, thus opening up possibilities to develop various tandem catalytic reactions. Among these reactions, the formation of heterocyclic compounds has attracted considerable attention. In this chapter, we will summarize the recent advances in the synthesis of heterocycles based on carbene coupling reactions. These reactions are roughly divided into six different types based on the reaction mechanism. The carbene precursors will include typical diazo compounds and N-tosylhydrazones, and also some less common carbene precursors, such as conjugated enynones and cyclopropenes. The metal catalysts will include Pd, Rh, Ir, Cu, and Co complexes." @default.
- W2803482054 created "2018-06-01" @default.
- W2803482054 creator A5013244136 @default.
- W2803482054 creator A5053883214 @default.
- W2803482054 date "2018-01-01" @default.
- W2803482054 modified "2023-10-14" @default.
- W2803482054 title "Synthesis of Heterocyclic Compounds Based on Transition-Metal-Catalyzed Carbene Coupling Reactions" @default.
- W2803482054 cites W1559701593 @default.
- W2803482054 cites W1770019281 @default.
- W2803482054 cites W1787868692 @default.
- W2803482054 cites W1839326775 @default.
- W2803482054 cites W1925221892 @default.
- W2803482054 cites W1943331823 @default.
- W2803482054 cites W1964610021 @default.
- W2803482054 cites W1967419891 @default.
- W2803482054 cites W1976419258 @default.
- W2803482054 cites W1976591534 @default.
- W2803482054 cites W1979497496 @default.
- W2803482054 cites W1984840652 @default.
- W2803482054 cites W1985702909 @default.
- W2803482054 cites W1988731149 @default.
- W2803482054 cites W1989273746 @default.
- W2803482054 cites W2001703055 @default.
- W2803482054 cites W2002643287 @default.
- W2803482054 cites W2004905245 @default.
- W2803482054 cites W2011251974 @default.
- W2803482054 cites W2015392501 @default.
- W2803482054 cites W2015962178 @default.
- W2803482054 cites W2024620782 @default.
- W2803482054 cites W2029708865 @default.
- W2803482054 cites W2050630113 @default.
- W2803482054 cites W2051510629 @default.
- W2803482054 cites W2054008144 @default.
- W2803482054 cites W2061892892 @default.
- W2803482054 cites W2062835578 @default.
- W2803482054 cites W2066523420 @default.
- W2803482054 cites W2086583179 @default.
- W2803482054 cites W2091473607 @default.
- W2803482054 cites W2093237076 @default.
- W2803482054 cites W2105898942 @default.
- W2803482054 cites W2111200702 @default.
- W2803482054 cites W2113311528 @default.
- W2803482054 cites W2124831012 @default.
- W2803482054 cites W2126151820 @default.
- W2803482054 cites W2126420609 @default.
- W2803482054 cites W2127442304 @default.
- W2803482054 cites W2141352953 @default.
- W2803482054 cites W2141657566 @default.
- W2803482054 cites W2142234470 @default.
- W2803482054 cites W2145183652 @default.
- W2803482054 cites W2152132247 @default.
- W2803482054 cites W2152680780 @default.
- W2803482054 cites W2154044432 @default.
- W2803482054 cites W2155531082 @default.
- W2803482054 cites W2155675561 @default.
- W2803482054 cites W2157370024 @default.
- W2803482054 cites W2158899039 @default.
- W2803482054 cites W2160574842 @default.
- W2803482054 cites W2162047307 @default.
- W2803482054 cites W2163773712 @default.
- W2803482054 cites W2164059448 @default.
- W2803482054 cites W2164854527 @default.
- W2803482054 cites W2171350759 @default.
- W2803482054 cites W2172304385 @default.
- W2803482054 cites W2175326861 @default.
- W2803482054 cites W2176205748 @default.
- W2803482054 cites W2176982028 @default.
- W2803482054 cites W2183388938 @default.
- W2803482054 cites W2199212773 @default.
- W2803482054 cites W2204357671 @default.
- W2803482054 cites W2222842705 @default.
- W2803482054 cites W2226309305 @default.
- W2803482054 cites W2259969681 @default.
- W2803482054 cites W2269286360 @default.
- W2803482054 cites W2275046656 @default.
- W2803482054 cites W2276575606 @default.
- W2803482054 cites W2278518034 @default.
- W2803482054 cites W2281782985 @default.
- W2803482054 cites W2296635481 @default.
- W2803482054 cites W2297001691 @default.
- W2803482054 cites W2308283129 @default.
- W2803482054 cites W2316248830 @default.
- W2803482054 cites W2317279620 @default.
- W2803482054 cites W2318009387 @default.
- W2803482054 cites W2319569391 @default.
- W2803482054 cites W2320478973 @default.
- W2803482054 cites W2323696407 @default.
- W2803482054 cites W2329895492 @default.
- W2803482054 cites W2334258901 @default.
- W2803482054 cites W2335663805 @default.
- W2803482054 cites W2336556579 @default.
- W2803482054 cites W2336762435 @default.
- W2803482054 cites W2337329226 @default.
- W2803482054 cites W2339051409 @default.
- W2803482054 cites W2343115761 @default.
- W2803482054 cites W2344734791 @default.
- W2803482054 cites W2396609756 @default.
- W2803482054 cites W2403774459 @default.