142066-41-9Relevant articles and documents
Highly chemo- and regio-selective hydroxylations of o- and m-substituted toluenes to benzyl alcohols with Cellulosimicrobium cellulans EB-8-4
Dai, Shiyao,Wu, Jinchuan,Wang, Zunsheng,Chen, Yongzheng,Li, Zhi
, p. 6919 - 6923 (2010)
Highly chemo- and regio-selective benzylic hydroxylations of o- and m-substituted toluenes were achieved with the easily available and easy-to-handle resting cells of Cellulosimicrobium cellulans EB-8-4 as biocatalysts, giving the corresponding benzyl alcohols as single product. Benzyl alcohols were obtained in 78-94% yield, demonstrating the first green, clean, and simple method for the preparation of benzyl alcohols via hydroxylations. Biotransformation of 4-methylbenzyl chloride with the same strain gave 4-methylbenzyl alcohol in 67-81% yield, suggesting a novel dehalogenation activity of the cells and providing a novel, green, and efficient method for the preparation of 4-methylbenzyl alcohol as well as the application potential in biodegradation of chlorine-containing aromatics.
Syntheses of 5-chlorouracils/thymines with 1-[phosphono(methyl/ difluoromethyl)]-1,2-unsaturated-moiety-substituted methyl groups at N(1) and human thymidine phosphorylase inhibitory activity
Birck, Matthew R.,Clinch, Keith,Gainsford, Graeme J.,Schramm, Vern L.,Tyler, Peter C.
scheme or table, p. 823 - 838 (2009/08/14)
By attaching (methyl)- or (difluoromethyl)-phosphonate groups to the 1-positions of ethene, cyclopentene or benzene, and attaching 1-(methyl)-5-chlorouracil or 1-(methyl)thymine groups to the corresponding 2-positions, compounds 1 - 5 were prepared as pot
Stereoselective synthesis of 1,2,2-trisubstituted indane derivatives using a tandem SN2-michael addition sequence
Gharpure, Santosh J.,Reddy, S. Raja Bhushan,Sanyal, Udishnu
, p. 1889 - 1892 (2008/03/13)
An efficient strategy is developed for the synthesis of 1,2,2-trisubstituted indane derivatives employing a tandem SN2- Michael reaction sequence. The method is extended towards the synthesis of spiroindanes and indanopiperidines. Georg Thieme Verlag Stuttgart.
Process for producing isochromanones and intermediates thereof
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Example 16, (2008/06/13)
(1) Methods for producing isochromanone compounds from o-xylene compounds as starting compounds through α-halogeno-o-xylene derivatives, α-cyano-o-xylene derivatives, and α-halogeno-α′-cyano-o-xylene derivatives, and (2) methods for producing isochromanone compounds from o-xylene compounds as starting compounds through α,α′-dihalogeno-o-xylene derivatives, α,α′-dihydroxy-o-xylene derivatives, α-halogeno-α′-hydroxy-o-xylene derivatives and α-cyano-α′-hydroxy-o-xylene derivatives, and methods for producing these intermediate compounds.
EPR investigation of persistent radicals produced from the photolysis of dibenzyl ketones adsorbed on ZSM-5 zeolites
Turro, Nicholas J.,Lei, Xue-Gong,Jockusch, Steffen,Li, Wei,Liu, Zhiqiang,Abrams, Lloyd,Ottaviani, M. Francesca
, p. 2606 - 2618 (2007/10/03)
Photolysis of ketones (1, 1-oMe, 2, 2-oMe, 3, and 4) adsorbed on ZSM-5 zeolites produces persistent carbon-centered radicals that can be readily observed by conventional steady-state EPR spectroscopy. The radicals are persistent for time periods of seconds to many hours depending on the supramolecular structure of the initial radical@zeolite complex and the diffusion and reaction dynamics of radicals produced by photolysis. The structures of the persistent radicals responsible for the observed EPR spectra are determined by a combination of alternate methods of generation of the same radical, by deuterium substitution, and by spectral simulation. A clear requirement for persistence is that the radicals produced by photolysis must either separate and diffuse from the external to the internal surface or be generated within the internal surface and separate and diffuse apart. The persistence of radicals located on the internal surface is the result of inhibition of radical-radical reactions. Radicals that are produced on the external surface and whose molecular structure prevents diffusion into the internal surface are transient because radical-radical reactions occur rapidly on the external surface. The reactions of the persistent radicals with oxygen and nitric oxide were directly studied in situ by EPR analysis. In the case of reaction with oxygen, persistent peroxy radicals are formed in high yield. The addition of nitric oxide scavenges persistent radicals and leads initially to a diamagnetic nitroso compound, which is transformed into a persistent nitroxide radical by further photolysis. The influence of variation of radical structure on transience/persistence is discussed and correlated with supramolecular structure and reactivity of the radicals and their parent ketones.
Orthocyclophanes. 1. Synthesis and Charaterization of 4>- and 5>Orthocyclophanes and Bicyclic Biscyclophanes
Lee, Woo Young,Park, Chang Hee,Kim, Young Dong
, p. 4074 - 4079 (2007/10/02)
4>- and 5>orthocyclophanes have been designed, synthesized and characterized.Dimetalation of bis(2-bromophenyl)methane (14) to the corresponding dilithio reagent 21, followed by reaction with aromatic dialdehydes bis(2-formylphen
A Convenient Total Synthesis of (+/-)-Bharatamine and (+/-)-Isobharatamine
Patil, Sharadbala D.,Mali, R. S.
, p. 360 - 362 (2007/10/02)
N,N-Dimethylbenzylamine (1) on lithiation with n-butyllithium followed by reaction with paraformaldehyde gives the 2-hydroxymethyl derivative (2). 2 on successive reactions with ClCOOEt, KCN and alc.KOH followed by cyclisation furnishes isochroman-3-one (3).Condensation of 3 with phenylethylamines (4a) and (4b), followed by cyclisation (PCl5), reduction (NaBH4), and debenzylation (EtOH-HCl) gives (+/-)-bharatamine (6c) and (+/-)-3-hydroxy-4-methoxy-5,6,13,13a-tetrahydro-8H-dibenzoquinolizine (isobharatamine, 6d), respectively in high yields.
