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- W4220782994 endingPage "153" @default.
- W4220782994 startingPage "59" @default.
- W4220782994 abstract "In recent years, metal-free catalysis has gained attention owing to its nontoxicity. Boron-based molecules play an important role in metal-free catalysis. An overview of triaryl or mixed aryl-alkylboranes, diarylborane, monoarylboranes, and borocations in catalysis is presented in this chapter. Lewis acidity and stability of trivalent boron compounds, especially tris(pentafluorophenyl)borane, made it as an increasingly useful catalyst in various organic transformations such as hydrogenation, hydrosilylation, hydroboration, reductive amination, N-alkylation, and so on. Apart from the Lewis acidity, borinic and boronic acids have the tendency to form reversible covalent interaction with groups such as carboxyl, hydroxyl, and carbonyl groups, which help them to activate the reagents in various organic transformations. Another important family of boron-based catalysis is borocation. Borocation, especially oxazaborolidines, plays a vital role in asymmetric catalysis such as Diels–Alder reaction, Michael addition, [3+2] cycloaddition, [2+2] cycloaddition, cyanosilylation of carbonyl compounds, etc. At the end of this chapter, the miscellaneous reactions catalyzed by boron reagents are summarized to illustrate the significance of boron catalysis." @default.
- W4220782994 created "2022-04-03" @default.
- W4220782994 creator A5030362403 @default.
- W4220782994 creator A5054736715 @default.
- W4220782994 date "2022-01-01" @default.
- W4220782994 modified "2023-09-26" @default.
- W4220782994 title "Applications of boron compounds in catalysis" @default.
- W4220782994 cites W1510374707 @default.
- W4220782994 cites W1711613787 @default.
- W4220782994 cites W1721211297 @default.
- W4220782994 cites W1854593855 @default.
- W4220782994 cites W1897198241 @default.
- W4220782994 cites W1931617008 @default.
- W4220782994 cites W1964885234 @default.
- W4220782994 cites W1965883576 @default.
- W4220782994 cites W1965988901 @default.
- W4220782994 cites W1966847399 @default.
- W4220782994 cites W1969333134 @default.
- W4220782994 cites W1971139155 @default.
- W4220782994 cites W1971373704 @default.
- W4220782994 cites W1974639070 @default.
- W4220782994 cites W1975457321 @default.
- W4220782994 cites W1975532762 @default.
- W4220782994 cites W1975788485 @default.
- W4220782994 cites W1979804093 @default.
- W4220782994 cites W1980565187 @default.
- W4220782994 cites W1980572232 @default.
- W4220782994 cites W1985715194 @default.
- W4220782994 cites W1986227128 @default.
- W4220782994 cites W1986228477 @default.
- W4220782994 cites W1988011709 @default.
- W4220782994 cites W1989818139 @default.
- W4220782994 cites W1995039108 @default.
- W4220782994 cites W1995277252 @default.
- W4220782994 cites W1996974614 @default.
- W4220782994 cites W1998893287 @default.
- W4220782994 cites W2000412424 @default.
- W4220782994 cites W2002066932 @default.
- W4220782994 cites W2003988428 @default.
- W4220782994 cites W2006537979 @default.
- W4220782994 cites W2008150228 @default.
- W4220782994 cites W2008691057 @default.
- W4220782994 cites W2010225964 @default.
- W4220782994 cites W2010790975 @default.
- W4220782994 cites W2010797442 @default.
- W4220782994 cites W2011519439 @default.
- W4220782994 cites W2012306698 @default.
- W4220782994 cites W2013283797 @default.
- W4220782994 cites W2019845529 @default.
- W4220782994 cites W2021427508 @default.
- W4220782994 cites W2021878208 @default.
- W4220782994 cites W2022213740 @default.
- W4220782994 cites W2022244698 @default.
- W4220782994 cites W2022930922 @default.
- W4220782994 cites W2023686448 @default.
- W4220782994 cites W2023756162 @default.
- W4220782994 cites W2023924290 @default.
- W4220782994 cites W2024126390 @default.
- W4220782994 cites W2024446293 @default.
- W4220782994 cites W2024664678 @default.
- W4220782994 cites W2026144804 @default.
- W4220782994 cites W2026985246 @default.
- W4220782994 cites W2030511154 @default.
- W4220782994 cites W2031245685 @default.
- W4220782994 cites W2035019453 @default.
- W4220782994 cites W2035417066 @default.
- W4220782994 cites W2035515056 @default.
- W4220782994 cites W2035855450 @default.
- W4220782994 cites W2036376341 @default.
- W4220782994 cites W2038712970 @default.
- W4220782994 cites W2040197204 @default.
- W4220782994 cites W2041647217 @default.
- W4220782994 cites W2045339115 @default.
- W4220782994 cites W2046141105 @default.
- W4220782994 cites W2048247933 @default.
- W4220782994 cites W2049852525 @default.
- W4220782994 cites W2051128662 @default.
- W4220782994 cites W2051382068 @default.
- W4220782994 cites W2054930916 @default.
- W4220782994 cites W2055237529 @default.
- W4220782994 cites W2056418521 @default.
- W4220782994 cites W2056652954 @default.
- W4220782994 cites W2057017771 @default.
- W4220782994 cites W2059683276 @default.
- W4220782994 cites W2060152301 @default.
- W4220782994 cites W2060517103 @default.
- W4220782994 cites W2065744658 @default.
- W4220782994 cites W2065891281 @default.
- W4220782994 cites W2068412684 @default.
- W4220782994 cites W2071033467 @default.
- W4220782994 cites W2071295591 @default.
- W4220782994 cites W2071904643 @default.
- W4220782994 cites W2073493603 @default.
- W4220782994 cites W2073563179 @default.
- W4220782994 cites W2076230764 @default.
- W4220782994 cites W2076564842 @default.
- W4220782994 cites W2079211064 @default.
- W4220782994 cites W2081654714 @default.