61266-34-0

Upstream product

• 38002-45-8 3-bromo-1-(trimethylsilyl)-1-propyne 
• 456-27-9 4-nitrobenzenediazonium tetrafluoroborate 
• 636-98-6 p-nitrobenzene iodide 
• 106-96-7 propargyl bromide 
• 61266-31-7 2-((3-(4-nitrophenyl)prop-2-yn-1-yl)oxy)tetrahydro-2H-pyran 
• 61266-32-8 3-(4-nitrophenyl)prop-2-yn-1-ol 

Downstream Products

• 1268381-72-1 C₁₁H₉NO₃S 
• 1268381-64-1 1-nitro-4-(3-(3-phenylprop-2-ynylsulfonyl)prop-1-ynyl)benzene 
• 1268381-67-4 (3-(4-methoxyphenyl)prop-2-ynyl)(3-(4-nitrophenyl)prop-2-ynyl)sulfane 
• 1268381-62-9 1-methoxy-4-(3-(3-(4-nitrophenyl)prop-2-ynylsulfonyl)prop-1-ynyl)benzene 
• 1268381-76-5 6-methoxy-4-(4-nitro-phenyl)-1,3-dihydro-naphtho[2,3-c]thiophene 2,2-dioxide 
• 1268381-68-5 (3-(4-nitrophenyl)prop-2-ynyl)(3-p-tolylprop-2-ynyl)sulfane 
• 1268381-63-0 1-methyl-4-(3-(3-(4-nitrophenyl)prop-2-ynylsulfonyl)prop-1-ynyl)benzene 
• 1268381-69-6 (3-(4-nitrophenyl)prop-2-ynyl)(3-phenylprop-2-ynyl)sulfane 
• 1312023-69-0 1-(4,4,4-trifluorobut-1-ynyl)-4-nitrobenzene 
• 1287769-24-7 4-iodo-3-(3-nitrophenyl)isoxazole 
• 1287769-12-3 benzyl 2,5-dihydro-4-iodo-3-(4-nitrophenyl)-2H-isoxazole-2-carboxylate 
• 1287768-92-6 isopropyl (3-(4-nitrophenyl)-2-propynyl)oxycarbamate 
• 1287768-77-7 benzyl (3-(4-nitrophenyl)-2-propynyl)oxycarbamate 
• 1287768-76-6 O-(3-(4-nitrophenyl)-2-propynyl)hydroxylamine 

Relevant academic research and scientific papers

A Pd NP-confined novel covalent organic polymer for catalytic applications

A novel unsymmetrical covalent organic polymer, COP (1), was designed and characterized using several analytical and spectroscopic techniques. COP (1) was synthesized via the nucleophilic substitution reaction of 2,4,6-trichloro-1,3,5-triazine with p-amin

Metal-free hydroamination of alkynes: A mild and concise synthesis of thiazolo[3,2- a ]indoles and their cytotoxic activity

A metal-free, mild and efficient method for the synthesis of thiazolo[3,2- a ]indoles has been developed starting from indoline-2-thiones. The reaction methodology involves first the formation of thermally labile 2-(prop-2-ynylthio)-1 H -indole intermedia

Visible light-mediated gold-catalysed carbon(sp2)-carbon(sp) cross-coupling

A dual photoredox and gold-catalysed cross-coupling reaction of alkynyltrimethylsilanes and aryldiazonium tetrafluoroborates is described. The reaction proceeds through visible-light mediated oxidative addition of aryldiazoniums, transmetalation of alkynyltrimethylsilanes and aryl-alkynyl reductive elimination. Exclusive selectivity for silyl-substituted alkynes is observed, with no reactivity observed for terminal alkynes.

Selectivity in Garratt-Braverman cyclization: An experimental and computational study

Bispropargyl sulfones equipped with aromatic rings of dissimilar nature were synthesized. Under basic conditions, these sulfones isomerized to the bisallenic sulfones, creating a competitive scenario between two alternate Garratt-Braverman (GB) cyclizatio

Iodocyclization of hydroxylamine derivatives based on the control of oxidative aromatization leading to 2,5-dihydroisoxazoles and isoxazoles

An efficient method for the synthesis of 2,5-dihydroisoxazoles and isoxazoles using iodocyclization of N-alkoxycarbonyl O-propargylic hydroxylamines has been developed. 2,5-Dihydro-4-iodoisoxazole underwent the cross-coupling reactions without aromatization to afford polyfunctionalized 2,5-dihydroisoxazoles. This process was applied to the preparation of valdecoxib and its 2,5-dihydro-derivative.