Reductive deprotection of allyl, benzyl and sulfonyl substituted alcohols, amines and amides using a naphthalene-catalysed lithiation
摘要:
The reaction of different protected alcohols, amines and amides with lithium and a catalytic amount of naphthalene (4 mol %) in THF at low temperature leads to their deprotection under very mild reaction conditions, the process being in many cases chemoselective. (C) 1997 Elsevier Science Ltd.
A system of potassium metal-crown ether-diglyme has been proved to be highly effective for reductive removal of the sulfonyl group from O-sulfonates or sulfonamides. The reaction proceeds even with mesylamides of dialkyl amines, which resist reductive cleavage by naphthalene radical anion. It has also been found that a simple combination of potassium metal or sodium-potassium alloy with isopropanol in diglyme or toluene is effective for the cleavage of dialkylamine sulfonamides which are relatively susceptible to reduction. In particular, the use of sodium-potassium alloy gave satisfactory results.
RADIATION-SENSITIVE COLORED COMPOSITION, COLORED CURED FILM, COLOR FILTER AND METHOD OF PRODUCING THE SAME, SOLID-STATE IMAGING DEVICE, LIQUID CRYSTAL DISPLAY APPARATUS, AND METHOD OF PRODUCING DYE
申请人:USHIJIMA Kenta
公开号:US20120235099A1
公开(公告)日:2012-09-20
The object of the present invention is to provide a radiation-sensitive colored composition which can supress the generation of the contamination of the device.
A radiation-sensitive colored composition including: (A) a dye containing of from 10 ppm to 1000 ppm of a halogen ion; (B) a polymerizable compound; and (C) a solvent.
PYRAZOLE DERIVATIVES AS CANNABINOID RECEPTOR 1 ANTAGONISTS
申请人:Fulp Alan Bradley
公开号:US20140107157A1
公开(公告)日:2014-04-17
The invention provides compounds capable of acting as antagonists at cannabanoid receptors according to the following formula: Such compounds may be used to treat conditions for which the cannabinoid receptor system has been implicated, such as obesity, liver disease, diabetes, pain, and inflammation.
arylalkylation of activated alkenes via hydrogen-atomtransfer and aryl migration strategy. The reaction was carried out through a radical-mediated continuous migration pathway using N-fluorosulfonamides as the alkyl source. The primary, secondary, and tertiary alkyl radicals formed by intramolecular hydrogen-atomtransfer proceeded smoothly. This methodology is an efficient approach for the synthesis of various
Copper-Catalyzed, N-Directed Csp<sup>3</sup>–H Trifluoromethylthiolation (−SCF<sub>3</sub>) and Trifluoromethylselenation (−SeCF<sub>3</sub>)
作者:Atanu Modak、Emily N. Pinter、Silas P. Cook
DOI:10.1021/jacs.9b10316
日期:2019.11.20
A direct and versatile copper-catalyzed trifluoromethylthiolation and trifluoromethylselenation of primary, secondary, and tertiary aliphatic C-H bonds was developed. The reaction provides direct access to molecules containing these emerging moieties in the presence of a wide range of common functional groups and in complex molecular environments.