نتایج جستجو برای: diazo coupling

تعداد نتایج: 153420  

Journal: :Neuron 1992
R C Malenka B Lancaster R S Zucker

The induction of long-term potentiation (LTP) in hippocampal CA1 pyramidal cells requires a rise in postsynaptic intracellular Ca2+ concentration ([Ca2+]i). To determine the time for which Ca2+ must remain elevated to induce LTP, the photolabile Ca2+ buffer diazo-4 was used to limit the duration of the rise in postsynaptic [Ca2+]i following a tetanus. The affinity of diazo-4 for Ca2+ increases ...

2017
Andrei Chirila Braja Gopal Das Nanda D Paul Bas de Bruin

A new protocol for the catalytic synthesis of cyclopropanes using electron-deficient alkenes is presented, which is catalysed by a series of affordable, easy to synthesise and highly active substituted cobalt(II) tetraaza[14]annulenes. These catalysts are compatible with the use of sodium tosylhydrazone salts as precursors to diazo compounds in one-pot catalytic transformations to afford the de...

2013
W. Kufer H. Scheer

A quantitative study o f the diazo reaction has been made with several bilirubins including a 2,3dihydrobilirubin and several phycorubins. The latter have been prepared from the integral phycocyanin of two cyanobacteria (Mastigocladus laminosus and Spirulina platensis), and from the phycocyanin subunits. These phycorubins have been subjected to the diazo reaction in order to test for the presen...

Journal: :Chemical communications 2014
Haibin Mao Zhongkai Tang Hongwen Hu Yixiang Cheng Wen-Hua Zheng Chengjian Zhu

A novel halogenation/semipinacol rearrangement of α-diazo alcohol catalyzed by Lewis base has been developed through a carbene-free mechanism. This semipinacol transposition, initiated by an electrophilic halogenation (X = Cl(+), Br(+), and I(+)) of diazo carbon event, furnished a convenient synthetic route for the efficient synthesis of α-halo-quaternary ketones under mild conditions.

Journal: :Organic letters 2007
Freeman M Wong Jianbo Wang Alvan C Hengge Weiming Wu

[reaction: see text] A large and normal nitrogen-15 kinetic isotope effect of 1.035 +/- 0.003 provides direct support for the proposed mechanism for the rhodium-catalyzed carbene formation from diazo compounds, which involves the fast formation of a metal-diazo complex followed by rate-limiting extrusion of N2. The large magnitude of the KIE indicates extensive C-N bond fission in the transitio...

2000
Zhongping Tan Zhaohui Qu Bei Chen Jianbo Wang

The diazo group of a series of a-diazo carbonyl compounds can be reduced to the corresponding CH2 group by Bu3SnH under Cu(acac)2-catalytic or photochemical conditions. The mechanistic aspects of this reaction were investigated in some detail, and a possible reaction pathway was discussed. q 2000 Elsevier Science Ltd. All rights reserved.

2005
E. G. GODFRIED

THE usual tests for bilirubinuria in routine clinical work are relatively insensitive; that this has long been recognised is shown by the various attempts to introduce more sensitive tests from time to time, but none of these has been widely employed. The object of this paper is to review once more the available methods, and to describe a simple yet very sensitive test which, in the opinion of ...

2015
Damon A. Parrish Stephanie Kramer G. Kenneth Windler David E. Chavez Philip W. Leonard

In the title compound, C5N6, all the atoms are approximately coplanar. In the crystal, mol-ecules are packed with short contact distances of 2.885 (2) (between the diazo N atom connected to the ring and a cyano N atom on a neighboring mol-ecule) and 3.012 (2) Å (between the terminal diazo N atom and an N atom of a neighboring imidazole ring).

Journal: :Chemistry and physics of lipids 2004
Douglass F Taber R Scott Hoerrner R Jason Herr D Mark Gleave Kazuo Kanai Richard Pina Qin Jiang Ming Xu

A general synthetic approach to the isoprostanes has been established, based on intermolecular aldol condensation of a diazo ketone with an unsaturated aldehyde, followed by cyclization of the resulting diazo ketone to the cyclopropane. Subsequent kinetic opening with thiophenol followed by further elaboration then leads to the isoprostane. The history of this approach and the details of its de...

Journal: :Journal of the American Chemical Society 2003
Richmond Sarpong Julius T Su Brian M Stoltz

A set of mild processes for the conversion of vinyl cyclopropyl diazo ketones to highly functionalized cycloheptadienones and vinyl cyclopentenones by use of a target-inspired tandem Wolff/Cope rearrangement sequence is described. A divergent reaction course of the vinyl cyclopropyl diazo ketone substrates under sono- or photochemical activation provides good to excellent yields (55-98%) of the...

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