930-66-5Relevant articles and documents
Cyclohexeno[3,4]cyclodec-1,5-diyne-3-ene: A Convenient Enediyne
Perrin, Charles L.,Shrinidhi, Annadka
supporting information, p. 6911 - 6915 (2021/09/14)
Enediynes are widely studied to understand their cycloaromatization and the trapping of the resulting p-dehydrobenzene diradical. However, few model substrates are known, and they are hard to synthesize and difficult to handle. Herein we report cyclohexen
Synthesis of Vinyl Chlorides via Triphosgene-Pyridine Activation of Ketones
Saputra, Mirza A.,Ngo, Ly,Kartika, Rendy
, p. 8815 - 8820 (2015/09/15)
Herein, we describe a mild method to prepare aliphatic and aromatic vinyl chlorides from their corresponding ketones via triphosgene-pyridine activation in dichloromethane at reflux. The mechanism of this reaction is proposed to involve formation of a put
Structure and Dynamic Features of an Intramolecular Frustrated Lewis Pair
Axenov, Kirill V.,Moemming, Cornelia M.,Kehr, Gerald,Froehlich, Roland,Erker, Gerhard
supporting information; experimental part, p. 14069 - 14073 (2011/02/23)
Di(mesityl)cyclohexenylphosphine undergoes hydroboration with Piers' borane [HB(C6F5)2] to yield the cyclohexylene- anellated frustrated Lewis pair 5. This P/B pair splits H2 with the formation of the product 4