73845-01-9

Upstream product

• 70-55-3 toluene-4-sulfonamide 
• 529-20-4 2-methylphenyl aldehyde 

Downstream Products

• 370565-64-3 ethyl 2-diazo-3-(N-tosyl)amino-3-(2-methylphenyl)propanoate 
• 501677-15-2 ethyl 2-diazo-3-oxo-5-(N-tosyl)amino-5-(2-methylphenyl)pentanoate 
• 1021427-38-2 (1R,2S,5R,8S,1'S)-5-(1'-p-tolylsulfonylamino-o-methylbenzyl)-1,11,11-trimethyl-3-oxa-6-azatricyclo[6.2.1.0^2,7]undec-6-en-4-one 
• 1021427-46-2 (1S,2R,5S,8R,1'R)-5-(1'-p-tolylsulfonylamino-o-methylbenzyl)-8,11,11-trimethyl-3-oxa-6-azatricyclo[6.2.1.0^2,7]undec-6-en-4-one 
• 1201851-53-7 (S,E)-N-(2-benzylidene-4-phenyl-1-o-tolylbut-3-ynyl)-4-methylbenzenesulfonamide 
• 1447965-11-8 2-(2-(2-methylphenyl)-3-tosyloxazolidin-4-yl)-1-phenylethanone 

Relevant academic research and scientific papers

Synthesis and biological evaluation of substituted phenyl azetidine-2-one sulphonyl derivatives as potential antimicrobial and antiviral agents

In the present study, we intend to synthesize a series of novel substituted phenyl azetidine-2-one sulphonyl derivatives. The entire set of derivatives 5 (a-t) were screened for in-vitro antibacterial, and antifungal activity, and among them eleven compou

A General Method for Imine Formation Using B(OCH2CF3)3

Tris(2,2,2-trifluoroethyl)borate [B(OCH2CF3)3] was found to be a mild and general reagent for the formation of a variety of imines by condensation of amides or amines with carbonyl compounds. N-Sulfinyl, N-toluenesulfonyl,

γcarbon Activation through N-Heterocyclic Carbene/Bronsted Acids Cooperative Catalysis: A Highly Enantioselective Route to γlactams

A carbon activation method that operates through N-heterocyclic carbene/Bronsted acid cooperative catalysis for highly enantioselective synthesis of γlactams is reported. The protocol allows the challenging remote carbon control of regioselectivity and en

Synthesis of cis-C-iodo-N-tosyl-aziridines using diiodomethyllithium: Reaction optimization, product scope and stability, and a protocol for selection of stationary phase for chromatography

The preparation of C-iodo-N-Ts-aziridines with excellent cis-diastereoselectivity has been achieved in high yields by the addition of diiodomethyllithium to N-tosylimines and N-tosylimine-HSO2Tol adducts. This addition-cyclization protocol succ

Screening of chiral phosphines as catalysts for the enantioselective [3+2] annulations of N-tosylimines with allenic esters

The use of chiral, binaphthyl-based phosphepines as catalysts improves previous results for the enantioselective [3+2] cyclisation reactions between allenic esters and N-tosylimines, both in terms of conversion rate and enantioselectivity. Pyrrolines bear

Highly diastereoselective and enantioselective direct organocatalytic anti-selective Mannich reactions employing N-tosylimines

Organocatalytic direct anti-selective Mannich reactions of O-TBS-hydroxyacetone with various N-tosylimines derived from aromatic aldehydes in the presence of L-threonine-derived catalyst afforded 1,2-amino alcohols in good yields and with enantioselectivi