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- W2891005010 endingPage "14574" @default.
- W2891005010 startingPage "14570" @default.
- W2891005010 abstract "Abstract The β‐borylborole 3 adds phenylacetylene in a [4+2]‐cycloaddition to give the boryl‐substituted 7‐boranorbornadiene derivative 4 b . Thermolysis (60 °C) results in a rearrangement with B−B coupling to give the tetraaryldiborane(4) 6 b . It splits dihydrogen with cleavage of the B−B bond. With the terminal acetylene 1‐pentyne the diborane(4) compound 6 b undergoes a rare 1,1‐diboration reaction to yield the respective geminal diborylalkene product 14 ." @default.
- W2891005010 created "2018-09-27" @default.
- W2891005010 creator A5004458229 @default.
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- W2891005010 creator A5034751002 @default.
- W2891005010 creator A5034807035 @default.
- W2891005010 creator A5048542589 @default.
- W2891005010 date "2018-10-08" @default.
- W2891005010 modified "2023-10-18" @default.
- W2891005010 title "The Borole Route to Reactive Pentafluorophenyl-Substituted Diboranes(4)" @default.
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