247089-85-6Relevant articles and documents
Preparation method of chiral optical pure p-toluenesulfinamide
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Paragraph 0014; 0041; 0055; 0056, (2018/09/13)
The invention discloses a preparation method of a chiral optical pure p-toluenesulfinamide. The method includes: subjecting sodium p-tolylsulfinate and an acyl chlorination reagent to acyl chlorination to obtain p-toluene sulfinyl chloride, then reacting
Preparation method of chiral optical pure p-toluene sulfamide
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Paragraph 0014; 0040; 0054; 0055, (2018/10/19)
The invention discloses a preparation method of chiral optical pure p-toluene sulfamide. The preparation method comprises the following steps: performing acylating chlorination by using sodium p-tolylsulfinate and an acylating chlorination reagent to obta
Enantioselective synthesis of diverse sulfinamides and sulfinylferrocenes from phenylglycine-derived chiral sulfinyl transfer agent
Han, Zhengxu S.,Meyer, Angelica M.,Xu, Yibo,Zhang, Yongda,Busch, Robert,Shen, Sherry,Grinberg, Nelu,Lu, Bruce Z.,Krishnamurthy, Dhileep,Senanayake, Chris H.
, p. 5480 - 5484 (2011/08/09)
A new chiral sulfinyl transfer auxiliary derived from readily available phenylglycine was developed. This auxiliary is utilized to synthesize a diverse array of alkyl- and arylsulfinamides and sulfinylferrocenes in high yields and excellent ee's. The desired products are produced in a one-pot sequence from the oxathiazolidine 2-oxide by two sequential nucleophilic additions that proceed in a stereospecific manner.