نتایج جستجو برای: substituted nitrile oxide

تعداد نتایج: 216363  

2008
Jie Xiao Hong Zhao

The title compound, C(37)H(26)N(2)O(2), was synthesized from 1,1'-methyl-enedinaphthalen-2-ol and 3-(bromo-methyl)-benzo-nitrile. The two naphthyl systems are almost perpendicular to each other [dihedral angle 83.3 (9)°] and the two cyano-benz-yloxy rings approximately parallel to each other [dihedral angle 15.5 (2)°].

Journal: :Angewandte Chemie 2015
Francis Belanger Charles E Chase Atsushi Endo Francis G Fang Jing Li Steven R Mathieu Annie Z Wilcoxen Huiming Zhang

Crystallization-induced diastereoselective transformation (CIDT) of an α-methyl nitrile completes an entirely non-chromatographic synthesis of the halichondrin B C14-C26 stereochemical array. The requisite α-methyl nitrile substrate is derived from D-quinic acid through a series of substrate-controlled stereoselective reactions via a number of crystalline intermediates that benefit from a rigid...

Journal: :Analytical Chemistry 2021

The nitrile imine-mediated tetrazole–ene cycloaddition is a widely used class of photoligation. Optimizing the reaction outcome requires detailed knowledge tetrazole photoactivation profile, which can only partially be ascertained from absorption spectroscopy, or otherwise involves laborious monitoring in solution. Photodissociation action spectroscopy (PDAS) combines advantages optical and mas...

2015
G. Kenneth Windler Brian L. Scott Neil C. Tomson Philip W. Leonard

In the title compound, C5HN7, the nitrile and azido substituents are close to being coplanar with the central ring. Mol-ecules in the crystal are linked via an N-H⋯N hydrogen bond to a nitrile acceptor, forming a chain extending along the c-axis direction.

Journal: :Chemical communications 2012
Michiko Sasaki Tomo Takegawa Hidaka Ikemoto Masatoshi Kawahata Kentaro Yamaguchi Kei Takeda

An α-chiral nitrile carbanion generated by deprotonation of enantioenriched O-carbamoyl cyanohydrin was trapped in situ with ethyl cyanoformate to give the corresponding ester derivative in 92% yield and 90 : 10 er, providing the first example of trapping of an α-chiral acyclic nitrile carbanion that has been considered to be very configurationally labile.

2013
Lei Bi Juejun Hu Peng Jiang Hyun Suk Kim Dong Hun Kim Mehmet Cengiz Onbasli Gerald F. Dionne Caroline A. Ross

Achieving monolithic integration of nonreciprocal photonic devices on semiconductor substrates has been long sought by the photonics research society. One way to achieve this goal is to deposit high quality magneto-optical oxide thin films on a semiconductor substrate. In this paper, we review our recent research activity on magneto-optical oxide thin films toward the goal of monolithic integra...

2001
Eduardo C. Meurer Luiz Alberto B. Moraes Marcos N. Eberlin

Gas phase reactions of mass-selected acylium ions [CH3–C ¢O (1), CH2¢CH–C ¢O (2), C6H5–C ¢O (3), and (CH3)2N–C ¢O (4)] with nitriles (CH3CN, C2H5CN, CH2¢CHCN, and C6H5CN) were investigated using pentaquadrupole multiple-stage mass spectrometry. In analogy with the solution behavior, the ions were found to react readily with benzonitrile by cyclization via double nitrile addition to form aromati...

Journal: :Chemical science 2015
Kenneth M Light Yasuaki Yamanaka Masafumi Odaka Edward I Solomon

Nitrile hydratases (NHases) are mononuclear nonheme enzymes that catalyze the hydration of nitriles to amides. NHase is unusual in that it utilizes a low-spin (LS) FeIII center and a unique ligand set comprised of two deprotonated backbone amides, cysteine-based sulfenic acid (RSO(H)) and sulfinic acid (RSO2-), and an unmodified cysteine trans to an exogenous ligand site. Electron paramagnetic ...

Journal: :The Journal of organic chemistry 2007
Nazario Martín Margarita Altable Salvatore Filippone Angel Martín-Domenech Roberto Martínez-Alvarez Margarita Suarez Marta E Plonska-Brzezinska Olena Lukoyanova Luis Echegoyen

Isoxazolino[4,5:1,2][60]- and -[70]fullerenes undergo an efficient retro-cycloaddition reaction to pristine fullerene by thermal treatment in the presence of an excess of a dienophile and Cu(II) catalysis, which can be selectively used in the presence of malonate or pyrrolidine cycloadducts. Trapping experiments using N-phenylmaleimide as dipolarophile have shown that the reaction mechanism occ...

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