《Unlocking the 5-exo Pathway with the AuI-Catalyzed Alkoxycyclization of 1,3-Dien-5-ynes》 was published in Chemistry – A European Journal in 2020. These research results belong to Virumbrales, Cintia; Suarez-Pantiga, Samuel; Marin-Luna, Marta; Silva Lopez, Carlos; Sanz, Roberto. Recommanded Product: 1530-32-1 The article mentions the following:
The first general regio- and stereoselective 5-exo gold(I)-catalyzed alkoxycyclization of a specific class of 1,5-enynes such as 1,3-dien-5-ynes was described, despite 1,5-enynes being known to almost invariably proceed via endo cyclizations under gold-catalysis. The configuration of the terminal alkene in the starting 1,3-dien-5-yne played a crucial role on the regiochem. outcome of the reaction. A wide variety of interesting alkoxy-functionalized alkylidenecyclopentenes was synthesized from 1-monosubstituted (E)-1,3-dien-5-ynes. On the contrary, the corresponding Z isomers evolve affording formal 6-endo cyclization products. In addition, mechanistic exploration supports a highly stabilized carbocation as a key intermediate instead of a highly constrained cyclopropyl gold carbene from E isomers, and also accounts for the well differentiated reactivity observed between both E/Z geometrical isomers as well as for the stereochem. outcome of the reaction. In the experiment, the researchers used Ethyltriphenylphosphonium bromide(cas: 1530-32-1Recommanded Product: 1530-32-1)
Ethyltriphenylphosphonium bromide(cas: 1530-32-1) is a phase transfer catalyst, used to accelerate the cure of phenolic-based epoxy resins, certain fluoroelastomer resins and thermosetting powder coatings. It is also used as catalysts in the synthesis of certain organic compounds and as a pharmaceutical intermediate.Recommanded Product: 1530-32-1
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary