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4-Hydroxy-4'-nitrobiphenyl | CAS:3916-44-7
4-Hydroxy-4'-nitrobiphenyl
  • 名称:4-羟基-4'-硝基联苯 | 4-Hydroxy-4'-nitrobiphenyl
  • CAS号:3916-44-7
  • 别名:
  • 分子式:C12H9NO3
  • 分子量:215.21
  • EINESC号:

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enolizable aldehydes with nitrostyrenes: computational study provides insight into the success of the catalyst.Daniel A DiRocco et al.Angewandte Chemie (International ed. in English), 51(10), 2391-2394 (2012-01-28) A one-pot synthesis of 7-phenylindolo[3,2-a]carbazoles from indoles and β-nitrostyrenes, via an unprecedented reaction sequence.Grégory Dupeyre et al.Organic & biomolecular chemistry, 9(22), 7780-7790 (2011-10-07) A microscopic technique to study kinetics and concentration-response of drug-induced caspase-3 activation on a single cell level.Jens Martin Werner et al.Journal of pharmacological and toxicological methods, 57(2), 131-137 (2007-12-19) Basic-functionalized recyclable ionic liquid catalyst: A solvent-free approach for Michael addition of 1,3-dicarbonyl compounds to nitroalkenes under ultrasound irradiation.Senthil Narayanaperumal et al.Ultrasonics sonochemistry, 20(3), 793-798 (2012-12-12) E-Combretastatin and E-resveratrol structural modifications: antimicrobial and cancer cell growth inhibitory beta-E-nitrostyrenes.Robin K Pettit et al.Bioorganic & medicinal chemistry, 17(18), 6606-6612 (2009-08-28) (S)-Proline-catalyzed nitro-Michael reactions: towards a better understanding of the catalytic mechanism and enantioselectivity.Hui Yang et al.Organic & biomolecular chemistry, 10(16), 3229-3235 (2012-03-10) Synthesis and pharmacological evaluation of novel beta-nitrostyrene derivatives as tyrosine kinase inhibitors with potent antiplatelet activity.Wei-Ya Wang et al.Biochemical pharmacology, 74(4), 601-611 (2007-07-03) trans-Beta-nitrostyrene derivatives as slow-binding inhibitors of protein tyrosine phosphatases.Junguk Park et al.Biochemistry, 43(47), 15014-15021 (2004-11-24) Asymmetric Michael reaction of acetaldehyde catalyzed by diphenylprolinol silyl ether.Yujiro Hayashi et al.Angewandte Chemie (International ed. in English), 47(25), 4722-4724 (2008-04-26) Synthesis of ribo-hexopyranoside- and altrose-based azacrown ethers and their application in an asymmetric Michael addition.Zsolt Rapi et al.Carbohydrate research, 365, 61-68 (2012-12-12) An unexpected promiscuous activity of 4-oxalocrotonate tautomerase: the cis-trans isomerisation of nitrostyrene.Ellen Zandvoort et al.Chembiochem : a European journal of chemical biology, 13(13), 1869-1873 (2012-08-02) Beta-nitrostyrene derivatives as potential antibacterial agents: a structure-property-activity relationship study.Nuno Milhazes et al.Bioorganic & medicinal chemistry, 14(12), 4078-4088 (2006-02-25) K3PO4-catalyzed regiospecific aminobromination of beta-nitrostyrene derivatives with N-bromoacetamide as aminobrominating agent.Zhan-Guo Chen et al.The Journal of organic chemistry, 75(6), 2085-2088 (2010-02-23) Comparison of the rapid pro-apoptotic effect of trans-beta-nitrostyrenes with delayed apoptosis induced by the standard agent 5-fluorouracil in colon cancer cells.Jens Martin Werner et al.Apoptosis : an international journal on programmed cell death, 12(1), 235-246 (2006-12-01) Promiscuous catalysis of asymmetric Michael-type additions of linear aldehydes to β-nitrostyrene by the proline-based enzyme 4-oxalocrotonate tautomerase.Yufeng Miao et al.Chembiochem : a European journal of chemical biology, 14(2), 191-194 (2013-01-11) Synthesis of strained cyclic peptides via an aza-Michael-acyl-transfer reaction cascade.Jochem P A Rutters et al.Chemical communications (Cambridge, England), 48(65), 8084-8086 (2012-07-07) Sequential catalytic role of bifunctional bicyclic guanidine in asymmetric phospha-Michael reaction.Bokun Cho et al.Organic & biomolecular chemistry, 9(12), 4550-4557 (2011-04-22) The synthesis and biologic evaluation of anti-platelet and cytotoxic β-nitrostyrenes.Pei-Wen Hsieh et al.Bioorganic & medicinal chemistry, 18(21), 7621-7627 (2010-09-21) Chiral squaramide derivatives are excellent hydrogen bond donor catalysts.Jeremiah P Malerich et al.Journal of the American Chemical Society, 130(44), 14416-14417 (2008-10-14) Bridging between organocatalysis and biocatalysis: asymmetric addition of acetaldehyde to β-nitrostyrenes catalyzed by a promiscuous proline-based tautomerase.Ellen Zandvoort et al.Angewandte Chemie (International ed. in English), 51(5), 1240-1243 (2011-12-23)
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