We present a simple and straightforward protocol for hydrochlorination of terminal arylalkynes to vinyl chlorides using hydrogen chloride under mild reaction conditions. This protocol does not involve any metal cataly...We present a simple and straightforward protocol for hydrochlorination of terminal arylalkynes to vinyl chlorides using hydrogen chloride under mild reaction conditions. This protocol does not involve any metal catalysts or additives. It is simple, inexpensive, and easy to prepare, and exhibits good reaction activity. The hydrochlorination proceeds smoothly to yield unique regioselective products via the Markovnikov addition rule.展开更多
An inexpensive BF3·Et20-catalyzed annulation reaction of arylacetaldehydes with arylalkynes has been developed. Various substituted phenylacetaldehydes and phenylacetylenes can undergo this reaction, producing co...An inexpensive BF3·Et20-catalyzed annulation reaction of arylacetaldehydes with arylalkynes has been developed. Various substituted phenylacetaldehydes and phenylacetylenes can undergo this reaction, producing corresponding α-aryl substituted naphthalene derivatives. Use of inexpensive and readily available BF3·Et20 catalyst constitutes the most attractive advantage of this transformation.展开更多
基金financial support from the National Basic Research Program of China(973 Program,No.2012CB720300)the Applied Basic Research Program of Bingtuan(No.2015AG001)the High-level Talent Scientific Research Project of Shihezi University(No.RCZX201405)
文摘We present a simple and straightforward protocol for hydrochlorination of terminal arylalkynes to vinyl chlorides using hydrogen chloride under mild reaction conditions. This protocol does not involve any metal catalysts or additives. It is simple, inexpensive, and easy to prepare, and exhibits good reaction activity. The hydrochlorination proceeds smoothly to yield unique regioselective products via the Markovnikov addition rule.
基金the financial supports from Sichuan Provincial Department of Education (11ZA108)National Natural Science Foundation of China (21202109 and 21072140)+1 种基金Special Funds of Sichuan Normal University for Sharing the Large Precision Equipments (DJ2012-07,DJ2011-16)Sichuan Normal University
文摘An inexpensive BF3·Et20-catalyzed annulation reaction of arylacetaldehydes with arylalkynes has been developed. Various substituted phenylacetaldehydes and phenylacetylenes can undergo this reaction, producing corresponding α-aryl substituted naphthalene derivatives. Use of inexpensive and readily available BF3·Et20 catalyst constitutes the most attractive advantage of this transformation.
