17674-16-7Relevant articles and documents
Activation and facile dealkylation of monooxides of 1,8-bis(alkylthio)naphthalene and 2,2′-bis(alkylthio)biphenyl with triflic anhydride via dithiadications
Shima, Hidetaka,Kobayashi, Ryoji,Furukawa, Naomichi
, p. 437 - 438 (1997)
Dithiadications bearing 1,8-bis(alkylthio)naphthalene 2A(a-e) and 2,2′-bis(alkylthio)biphenyl 2B(a-e) structure undergo either the facile deprotonation from the methyl group or dealkylation from the methylene groups by the triflate anion. Dications 2A(a) and 2B(a) having methyl groups were deprotonated readily to afford cyclic sulfonium salts 3A(a) and 3B(a). However, dithiadications 2A(b-e) and 2B(b-e) having ethyl, propyl, isopropyl and benzyl groups were readily dealkylated even at -45°C to give thiasulfonium salts 4A(b-e) and 4B(b-e) and alkyl triflates 5(a-e) in good yields. The intermediary formation of dithiadications 2A(a-e) and 2B(a-e) were confirmed by direct observation using NMR spectroscopy, D-labelled experiments and trapping experiments.
Trifluoromethyl Nonaflate: A Practical Trifluoromethoxylating Reagent and its Application to the Regio- and Stereoselective Synthesis of Trifluoromethoxylated Alkenes
Hammond, Gerald B.,Kumon, Tatsuya,Lu, Zhichao,Umemoto, Teruo
supporting information, p. 16171 - 16177 (2021/06/27)
The trifluoromethoxy group has elicited much interest among drug and agrochemical discovery teams because of its unique properties. We developed trifluoromethyl nonafluorobutanesulfonate (nonaflate), TFNf, an easy-to-handle, bench-stable, reactive, and scalable trifluoromethoxylating reagent. TFNf is easily and safely prepared in a simple process in large scale and the nonaflyl part of TFNf can easily be recovered as nonaflyl fluoride after usage and recycled. The synthetic potency of TFNf was showcased with the underexplored synthesis of various trifluoromethoxylated alkenes, through a high regio- and stereoselective hydro(halo)trifluoromethoxylation of alkyne derivatives such as haloalkynes, alkynyl esters, and alkynyl sulfones. The synthetic merits of TFNf were further underscored with a high-yielding and smooth nucleophilic trifluoromethoxylation of alkyl triflates/bromides and primary/secondary alcohols.
Development of triazine-based benzylating reagents possessing T-butyl group on the triazine core: Thermally controllable reagents for the initiation of reaction
Karuo, Yukiko,Yamada, Kohei,Kunishima, Munetaka
, p. 303 - 308 (2018/03/09)
Benzylating reagents, 4-(4,6-di-t-butyl-1,3,5-triazin-2-yl)-4-benzylmorpholinium triflate, and related derivatives have been developed. The reagents release benzyl triflate as a benzyl cation equivalent upon heating the solution to 40°C under neutral conditions. The O-benzylation of alcohols using a stoichiometric amount of these reagents afforded corresponding benzyl ethers in good to high yields. This was due to the presence of a bulky t-butyl group on the triazine ring of these reagents that prevents the consumption of benzyl triflate via a side reaction with a morpholinotriazine derivative.
β-alkoxy-γ-amino aldehydes by internal redox ring cleavages of carbohydrate-derived enantiopure 1,2-oxazines and preparation of heterocycles with aminopolyol side chain
Al-Harrasi, Ahmed,Bouche, Lea,Zimmer, Reinhold,Reissig, Hans-Ulrich
experimental part, p. 109 - 118 (2011/03/19)
N-Methylation of syn- or anti-configured 3,6-dihydro-2H-1,2-oxazines and subsequent treatment with triethylamine smoothly provided enantiopure α,β-unsaturated β-alkoxy-γ-amino aldehydes bearing different protected diol, triol, or tetrol side chains in goo
