5075-33-2Relevant academic research and scientific papers
Gold-Catalyzed Rearrangement of Alkynyl Donor-Acceptor Cyclopropanes to Construct Highly Functionalized Alkylidenecyclopentenes
Chen, Huiyu,Zhang, Jing,Wang, David Zhigang
supporting information, p. 2098 - 2101 (2015/05/13)
A gold-catalyzed 1,7-addition-cyclization-elimination cascade sequence performed on a range of alkynyl-substituted donor-acceptor-type cyclopropanes provides facile entry to highly functionalized exo-alkylidenecyclopentenes under very mild conditions. Iso
Cycloaddition Reactions of Allenyl Cations with Cyclopentadiene
Mayr, Herbert,Halberstadt-Kausch, Inge K.
, p. 3479 - 3515 (2007/10/02)
Propargyl halides R1-C=-C-CR2R3X (14) and cyclopentadiene react with zinc halide catalysis in ether/dichloromethane solution to give 3-halogenobicycloocta-2,6-dienes 13 (R1 = alkyl) or 5-(α-halogenobenzylidene)norbornenes 15 (R1 = aryl).The reactions are interpreted by stepwise - and -cycloadditions of intermediate allenyl cations 1, proceeding via propargylcyclopentenyl cations 5 and bicyclic vinyl cations 9 or 12.If the reactions are initiated by equimolar amounts of silver trifluoroacetate, quenching products of all postulated intermediates are isolated.The relative energies of the intermediate carbenium ions are estimated on the basis of force field calculations and of gas phase stabilities of simple carbocations.Stereochemical studies indicate that the addition reactions proceed via the compact transition state 42 rather than 41.The zinc chloride catalysed reaction of propargyl chloride 14e with cyclopentadiene yields the 2:1 product 17 (structurally assigned by X ray analysis) in addition to the 1:1 product 15e.The formation of 17 is rationalised by a -cycloaddition of allenyl cation 1 with cyclopentadiene.
