1200697-34-2Relevant articles and documents
Enabling the Rearrangement of Unactivated Allenes to 1,3-Dienes by Use of a Palladium (0)/Boric Acid System
Al-Jawaheri, Yassir,Turner, Matthew,Kimber, Marc C.
supporting information, p. 2329 - 2336 (2018/06/15)
A redox neutral rearrangement of an allene to a 1,3-diene by means of a unique palladium hydride complex is reported. The palladium hydride complex is generated from a simple Pd 0 source and boric acid [B(OH) 3 ], which is typically identified as a waste by-product of the Suzuki-Miyaura reaction. A mechanism for this transformation using this novel palladium hydride complex is presented; using a direct sample loop and flow injection ESI-HRMS analysis we have detected and identified key π-allylpalladium complexes that support the addition of the palladium hydride complex to the allene.
Generation of allenic/propargylic zirconium complexes and subsequent cross-coupling reactions: A facile synthesis of multisubstituted allenes
Zhang, Hao,Fu, Xiaoping,Chen, Jingjin,Wang, Erjuan,Liu, Yuanhong,Li, Yuxue
supporting information; experimental part, p. 9351 - 9358 (2010/03/04)
(Chemical Equation Presented) The β-alkoxide elimination reaction of propargylic ether with Negishi reagent leads to allenes and/or alkynes after hydrolysis. The product distribution is highly dependent on the substitution pattern of starting propargylic