131186-52-2Relevant articles and documents
Selective synthesis of enol ethers: Via nickel-catalyzed cross coupling of α-oxy-vinylsulfones with alkylzinc reagents
Gong, Liang,Zhang, Qian,Xie, Demeng,Zhang, Wei,Xu, Shi-Yang,Zhang, Xia,Niu, Dawen
, p. 12273 - 12276 (2021/11/30)
We describe here a Ni-catalyzed Negishi coupling reaction to prepare 1,2-dialkyl enol ethers in a stereoconvergent fashion. This method employs readily available and bench-stable α-oxy-vinylsulfones as electrophiles. The C-sulfone bond in the α-oxy-vinylsulfone motif is cleaved chemoselectively in these reactions. The mild conditions are tolerant of a variety of functional groups on both partners, thus representing a general strategy for enol ether synthesis. This unique reactivity of α-oxy-vinylsulfones indicates their further application as electrophilic partners in cross-coupling reactions.
Sulphone-mediated cyclobutanone to α-alkoxy-cyclopentanone ring expansion reactions; scope, limitations and applications
Finch, Harry,Mjalli, Adnan M. M.,Montana, John G.,Roberts, Stanley M.,Taylor, Richard J. K.
, p. 4925 - 4950 (2007/10/02)
The bicycloalkanones (1)-(3) were treated with the lithiated sulphone (4) to give the ring expanded α-methoxyketones (12), (14) and (16) generally as a mixture of epimers. The same bicycloalkanones furnished the α-benzyloxyketones (13), (15), and (17) on reaction with reagent (5). The ketone (3) reacted with the sulphone anion (6) to give, after Lewis acid treatment, the α-allyloxycyclopentanone derivatives (27a) and (27b) and one of these compounds (27b) was transformed into the ether (31). The bicycloheptanone (20) was converted into four ring-expanded products (22a), (22b), (24a) and (24b) and one of the compounds (24a) was used to synthesise the prostacyclin analogue (36). A brief study was made of the mechanism of the Lewis-acid catalysed rearrangement of the intermediate hydroxy sulphone to the ring-expanded compounds.
