نتایج جستجو برای: secondary reaction

تعداد نتایج: 701613  

Journal: :Organic letters 2001
D A Evans E Hu J S Tedrow

[reaction: see text] The L-callipeltose subunit of L-callipeltoside A has been synthesized in 10 steps and 13% overall yield from D-threonine. The key steps are a highly diastereoselective Felkin anti aldol addition to a methyl ketone and a selective methylation of a secondary alcohol in the presence of a secondary carbamate.

Journal: :Dalton transactions 2014
Raju Poreddy Eduardo J García-Suárez Anders Riisager Søren Kegnæs

Silver nanoparticles supported on alumina were prepared and tested in the catalytic reduction of various imines to primary and secondary amines and were shown to be exceptionally active and chemoselective. Furthermore, the catalytic activity of the prepared nanocatalyst was also tested in the synthesis of secondary amines from primary amines in a tandem reaction protocol (oxidation-imination-re...

Journal: :Chemical communications 2011
Li Zhang Ji-Hu Su Sujing Wang Changfeng Wan Zhenggen Zha Jiangfeng Du Zhiyong Wang

Direct electrochemical synthesis of sulfonyl amidines from aliphatic amines and sulfonyl azides was realized with good to excellent yields. Traditional tertiary amine substrates were broadened to secondary and primary amines. The reaction intermediates were observed and a reaction mechanism was proposed and discussed.

2017
Kadriye Terzioğlu Dane Ediger Raziye Tülümen Öztürk Eda Durmuş Mehmet Fethi Alışır

Kounis syndrome is an allergy-associated acute coronary syndrome, which develops secondary to mast cell activation in coronary arteries due to hypersensitivity or anaphylactoid reaction (1). The triggering factors may be various drugs, food, environmental exposure, and intracoronary stents (2–4). In this case report, an extraordinary case of Kounis syndrome (acute myocardial infarction with con...

Journal: :Organic & biomolecular chemistry 2009
Baoda Lin Miaochang Liu Zhishi Ye Jinchang Ding Huayue Wu Jiang Cheng

A copper-catalyzed C-N bond forming reaction among aryl siloxane and primary, secondary amines as well as amides has been described. The reaction was conducted in the presence of P(C6F5)3 and 4 A molecular sieves in CH2Cl2 at room temperature under O2. A catalytic amount of TBAF was employed to activate aryl siloxanes.

Journal: :The Journal of organic chemistry 2016
Wei Ding Liang-Qiu Lu Jing Liu Dan Liu Hai-Tao Song Wen-Jing Xiao

An intermolecular radical-radical cross-coupling reaction of secondary and tertiary amines with aryl ketones and aldehydes has been developed using visible light photoredox catalysis. This reaction provides an efficient and straightforward approach to some useful 1,2-amino alcohols in moderate to good yields under mild conditions.

Journal: :Circulation 1981
J Moss N R Fahmy N Sunder M A Beaven

A 28-year-old female undergoing elective total hip replacement experienced an anaphylactic reaction to succinylcholine. Hemodynamics, plasma histamine and catecholamines were measured. The tachycardia experienced during the reaction appeared to be secondary to the sympathoadrenal response rather than a direct chronotropic effect of histamine.

Journal: :Postgraduate medical journal 1977
A S Narayana D G Kelly F A Duff

The first case of leiomyosarcoma of the urinary bladder associated with leukaemoid reaction is herein presented. There was no secondary involvement of bone marrow to explain the leukaemoid reaction. It may have been due either to tumour necrosis or to an unknown humoral substance elaborated by the tumour.

Journal: :Chemical communications 2013
John D Nguyen Barbara Reiss Chunhui Dai Corey R J Stephenson

Herein we report a one-pot deoxygenation protocol for primary and secondary alcohols developed via the combination of the Garegg-Samuelsson reaction, visible light-photoredox catalysis, and flow chemistry. This procedure is characterized by mild reaction conditions, easy-to-handle reactants and reagents, excellent functional group tolerance, and good yields.

Journal: :Chemical communications 2012
Julien Genovino Bharat Lagu Yaping Wang B Barry Touré

The first TiCl(4)-mediated condensation of secondary amides with aldehydes and ketones has been achieved. The reaction proceeds at room temperature and is complete within 5 h in most cases. The optimized procedure used 5 equiv of an amine base hinting that the in situ activation of both the amide and the Lewis acid is required. The reaction affords polysubstituted (E)-enamides.

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