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Alkyne 1,1‐Hydroboration to a Reactive Frustrated P/B‐H Lewis Pair
Author(s) -
Škoch Karel,
Daniliuc Constantin G.,
Kehr Gerald,
Erker Gerhard
Publication year - 2021
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.202014562
Subject(s) - borane , hydroboration , chemistry , alkyne , frustrated lewis pair , boranes , ylide , derivative (finance) , adduct , medicinal chemistry , stereochemistry , lewis acids and bases , organic chemistry , catalysis , boron , financial economics , economics
The Mes 2 P‐C≡C‐SiMe 3 alkyne reacts with the borane H 2 B‐Fmes by means of a rare 1,1‐hydroboration reaction to give an unsaturated C 2 ‐bridged frustrated P/B‐H Lewis pair. Most of its reactions are determined by the presence of the B‐H functionality at the FLP function and the activated connecting carbon‐carbon double bond. It reduces carbon monoxide to the formyl stage. With nitriles it reacts in an extraordinary way: it undergoes a reaction sequence that eventually results in the formation of a P‐substituted dihydro‐1,2‐azaborole derivative. Several similar examples were found. In one case a P‐ylide was isolated that was related to an intermediate of the reaction sequence. It subsequently opened in an alternative way to give an alkenyl borane product.