Synthesis of diverse ethoxyformacetal oligomers. Toward libraries of metal-coordinating unnatural biopolymers
摘要:
An expedient two-step iterative protocol for the solution-phase elaboration of ethoxyformacetal oligomers is described. A set of four O,S-thioformacetal donor monomers, with diverse chiral side-chains, were coupled using NIS/TfOH activation to afford three model tetramers. (C) 1997 Published by Elsevier Science Ltd.
Synthesis of diverse ethoxyformacetal oligomers. Toward libraries of metal-coordinating unnatural biopolymers
摘要:
An expedient two-step iterative protocol for the solution-phase elaboration of ethoxyformacetal oligomers is described. A set of four O,S-thioformacetal donor monomers, with diverse chiral side-chains, were coupled using NIS/TfOH activation to afford three model tetramers. (C) 1997 Published by Elsevier Science Ltd.
Reaction of the N-(α-chloroalkyloxycarbonyl)pyrrolidines 1 with lithium powder and a catalytic amount of 4,4′-di-tert-butylbiphenyl (DTBB, 2.5 mol-%) in the presence of different electrophiles [iBuCHO, tBuCHO, PhCHO, Et2CO, (CH2)5CO, PhCOMe, Ph2CO, Me3SiCl], in THF at temperatures ranging between –78 and –60°C leads, after hydrolysis with water, to the expected functionalized carbamates 2. Deprotection
Disclosed herein are cannabinoid receptor ligands of formula (I)
wherein A
1
, A
5
, R
x
, X
4
, and z are as defined in the specification. Compositions comprising such compounds, and methods for treating conditions and disorders using such compounds and compositions are also disclosed.
N-(Chloromethyloxycarbonyl)pyrrolidine as a source of the HOCH2− synthon
作者:Albert Guijarro、Miguel Yus
DOI:10.1016/0040-4039(96)01133-1
日期:1996.7
The reaction of N-(chloromethyloxycarbonyl)pyrrolidine (1) with lithium powder and a catalytic amount of DTBB (2.5 mol %) in the presence of different electrophiles [Me3SiCl, BujCHO, ButCHO, PhCHO, Et2CO, (CH2)5CO, PhCOMe, Ph2CO] in THF at −78°C leads, after hydrolysis with water, to the expected functionalised carbamates 2. Deprotection of the acetophenone derivative 2g with DIBALH at THF reflux yields
的反应Ñ(chloromethyloxycarbonyl)吡咯烷( - 1在不同的亲电子[我的存在锂粉末和DTBB催化量(2.5摩尔%))3的SiCl,卜Ĵ CHO,卜吨CHO,苯甲醛,等2 CO ,-(CH 2)5 CO,PhCOMe,Ph 2 CO]在THF中于-78°C水解后,可生成预期的官能化氨基甲酸酯2。在THF回流下,用DIBALH对苯乙酮衍生物2g进行脱保护,水解后得到相应的1,2-二醇3g。
[EN] PROCESS FOR REDUCING THE OXYGEN CONTENT OF BIOMASS USING VANADIUM-BASED CATALYSTS<br/>[FR] PROCÉDÉ POUR RÉDUIRE LA TENEUR EN OXYGÈNE DE LA BIOMASSE À L'AIDE DE CATALYSEURS À BASE DE VANADIUM
申请人:UNIV DANMARKS TEKNISKE
公开号:WO2016101958A1
公开(公告)日:2016-06-30
The present invention concerns a process for converting biomass into useful organic building blocks for the chemical industry. The process involves the use of vanadium-based catalysts of the formula Aα+a(VvXxR1yR2z)α*a-, which may be readily prepared from industrial vanadium compounds, for converting a polyol in a solvent.
The present invention relates to novel bicyclic enamino(thio)carbonyl compounds, to processes for their preparation and to their use for controlling animal pests, especially arthropods, in particular insects.