Wang, Wei published the artcileNickel-Catalyzed One-Pot Carbonylative Synthesis of 2-Mono- and 2,3-Disubstituted Thiochromenones from 2-Bromobenzenesulfonyl Chlorides and Alkynes, Application In Synthesis of 21286-54-4, the publication is Organic Letters (2021), 23(16), 6589-6593, database is CAplus and MEDLINE.
A nickel-catalyzed one-pot carbonylation reaction of 2-bromobenzenesulfonyl chlorides I (R = H, Me, OMe; R1 = H, OMe; RR1 = -OCH2O-, -O(CH2)2O-) with alkynes R2CCR3 (R2 = Me, Ph, 2-thienyl, etc.; R3 = Ph, 3-thienyl, 2-naphthyl, etc.) for the synthesis of thiochromenones II has been established. The alkynes were suitable substrates in this carbonylative transformation, and a broad range of 2-mono- and 2,3-disubstituted thiochromenone products II were obtained in moderate to good yields with quite high functional group compatibility. Notably, this procedure presents the first example of nickel-catalyzed carbonylative synthesis of thiochromenones II with 2-bromobenzenesulfonyl chlorides as a promising sulfur precursor.
Organic Letters published new progress about 21286-54-4. 21286-54-4 belongs to chlorides-buliding-blocks, auxiliary class Chiral,Chloride,Sulfonyl chlorides,Aliphatic cyclic hydrocarbon,Ketone, name is ((1S,4R)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonyl chloride, and the molecular formula is C7H9BO3, Application In Synthesis of 21286-54-4.
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