Substitution reactions of alkanesulfonyl derivatives: direct substitution vs. elimination-addition mechanisms in substitution reactions of alkyl .alpha.-disulfones
Copper-Catalyzed Difunctionalization of Allenes with Sulfonyl Iodides Leading to (<i>E</i>)-α-Iodomethyl Vinylsulfones
作者:Ning Lu、Zhiguo Zhang、Nana Ma、Conghui Wu、Guisheng Zhang、Qingfeng Liu、Tongxin Liu
DOI:10.1021/acs.orglett.8b01765
日期:2018.7.20
A highly regioselective iodosulfonylation of allenes in the presence of CuI and 1,10-phenanthroline has been developed for the synthesis of various useful (E)-α-iodomethyl vinylsulfones in moderate to excellent yields. This practical reaction is fast, operationally simple, and in particular, proceeds under very mild conditions to afford the target products with high regio- and stereoselectivity. The
Enantioselective Synthesis of Cyclopropanone Equivalents and Application to the Formation of Chiral β‐Lactams
作者:Christopher M. Poteat、Yujin Jang、Myunggi Jung、J. Drake Johnson、Rachel G. Williams、Vincent N. G. Lindsay
DOI:10.1002/anie.202006786
日期:2020.10.12
derivatives have long been considered unsustainable synthetic intermediates because of their extreme strain and kinetic instability. Reported here is the enantioselective synthesis of 1‐sulfonylcyclopropanols, as stable yet powerful equivalents of the corresponding cyclopropanone derivatives, by α‐hydroxylation of sulfonylcyclopropanes using a bis(silyl) peroxide as the electrophilic oxygen source. This
New benzimidazoloquinones substituted at 2-position by a sulfonyl group have been synthesized via a final microwave assisted step using 2-chloromethyl-1,5,6-trimethylbenzimidazole-4,7-dione 7 as starting material.
A series of highly functionalized quinones was prepared by an original reaction of 2,3-bis(chloromethyl)-1,4-dimethoxyanthraquinone (6) with various nitronate anions under electron transfer reaction conditions.
Electrochemical Radical–Radical Cross-Coupling Approach between Sodium Sulfinates and 2<i>H</i>-Indazoles to 3-Sulfonylated 2<i>H</i>-Indazoles
作者:Wansoo Kim、Hun Young Kim、Kyungsoo Oh
DOI:10.1021/acs.orglett.0c02144
日期:2020.8.21
A direct cross-coupling between sodium sulfinates and 2H-indazoles has been developed under electrochemical conditions. The utilization of a graphite anode and platinum cathode in an undivided cell with a constant current of 7 mA allowed the concurrent oxidations of sulfinates and 2H-indazoles to sulfonyl radical and radical cationic 2H-indazoles, facilitating the direct radical–radical coupling strategy