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9月, 2013の投稿を表示しています
Communication Substituent Dependent Reactivity of Ni(II) Complexes Towards Air Chandan Mukherjee  and     Samir Ghorai    Dalton Trans. , 2013, Accepted Manuscript DOI:  10.1039/C3DT52072B Received 31 Jul 2013, Accepted 26 Sep 2013 First published online 26 Sep 2013 | | Share on citeulike | Share on facebook | Share on twitter | | More PDF Rich HTML    Send PDF to Kindle Download Citation BibTex   EndNote   MEDLINE   ProCite   ReferenceManager   RefWorks   RIS   Request Permissions Abstract Cited by Related Content Metrics Radical¯containing Ni(II) complexes (1 and 2) without and with tert¯butyl substituent at the salicylidene unit have been synthesized. Complex 2 underwent ligand centered C¯H activation by aerial oxygen and formed corresponding amide complex (2a). Position of the Ni center above the salen plane was respo...
Geometric and Electronic Structure Contributions to Function in Non-heme Iron Enzymes ACS ActiveView PDF Hi-Res Print, Annotate, Reference QuickView PDF [2750 KB] PDF w/ Links [1101 KB] Full Text HTML Abstract Figures Reference QuickView Add to ACS ChemWorx Edward I. Solomon * , Kenneth M. Light , Lei V. Liu , Martin Srnec , and Shaun D. Wong Department of Chemistry, Stanford University , Stanford, California 94305-5080, United States Acc. Chem. Res. , Article ASAP DOI: 10.1021/ar400149m Publication Date (Web): September 26, 2013 Copyright © 2013 American Chemical Society Abstract Mononuclear non-heme Fe (NHFe) enzymes play key roles in DNA repair, the biosynthesis of antibiotics, the response to hypoxia, cancer therapy, and many other biological processes. These enzymes catalyze a diverse range of oxidation reactions, including hydroxylation, halogenation, ring closure, desaturation, and electrophilic...
Rescuing Auxotrophic Microorganisms with Nonenzymatic Chemistry † Dr. Yunmi Lee 1 ,  Afoma Umeano 2 ,  Prof. Emily P. Balskus 2,* Article first published online: 20 SEP 2013 DOI: 10.1002/anie.201307033 Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Keywords: auxotrophy; hydroxylation; metabolism; microorganisms; protecting groups Organic chemistry to the rescue : Two unrelated nonenzymatic chemical reactions can support the growth of auxotrophic  E. coli  strains by generating essential nutrients in situ. These biocompatible reactions, which take place in the presence of the organisms and are designed to interface with cellular metabolic processes, provide a means of linking the growth of an organism to the success of a nonbiological chemical transformation. View Full Article with Supporting Information (HTML)   Get PDF (1152K)
Perspective Activation of carbon–hydrogen bonds and dihydrogen by 1,2-CH-addition across metal–heteroatom bonds Joanna R. Webb , a      Samantha A. Burgess , b    Thomas R. Cundari * c  and     T. Brent Gunnoe * b    Show Affiliations Dalton Trans. , 2013, Advance Article DOI:  10.1039/C3DT52164H Received 08 Aug 2013, Accepted 13 Sep 2013 First published online 25 Sep 2013 | | Share on citeulike | Share on facebook | Share on twitter | | More PDF Rich HTML    Send PDF to Kindle Download Citation BibTex   EndNote   MEDLINE   ProCite   ReferenceManager   RefWorks   RIS   Request Permissions Abstract Cited by Related Content Metrics   The controlled conversion of hydrocarbons to functionalized products requires selective C–H bond cleavage. This perspective provides an overview of 1,2-CH-addition o...
Communication You have full text access to this content Comparison of the Reactivity of Nonheme Iron(IV)–Oxo versus Iron(IV)–Imido Complexes: Which is the Better Oxidant? † Anil Kumar Vardhaman 1 ,  Prasenjit Barman 1 ,  Suresh Kumar 2 ,  Dr. Chivukula V. Sastri 1,* ,  Dr. Devesh Kumar 2,* ,  Dr. Sam P. de Visser 3,* Article first published online: 25 SEP 2013 DOI: 10.1002/anie.201305370 Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Keywords:  C H activation; enzyme models; imido ligands; iron; sulfoxidation Which is better?  The first detailed study into a comparison of the reactivity of nonheme iron(IV)–imido versus nonheme iron(IV)-oxo intermediates with substrates is presented. The iron(IV)–imido variant reacts with sulfides five times faster than iron(IV)–oxo, whereas the reverse trend is observed for hydrogen atom abstraction. These observed trends are analyzed and explained. View...
Communication Catalytic and regiospecific extradiol cleavage of catechol by a biomimetic iron complex Sayanti Chatterjee , a      Debobrata Sheet a  and   Tapan Kanti Paine * a    Show Affiliations Chem. Commun. , 2013, Advance Article DOI:  10.1039/C3CC44124E Received 01 Jun 2013, Accepted 10 Sep 2013 First published online 10 Sep 2013 | | Share on citeulike | Share on facebook | Share on twitter | | More PDF Rich HTML    Send PDF to Kindle Download Citation BibTex   EndNote   MEDLINE   ProCite   ReferenceManager   RefWorks   RIS   Request Permissions Abstract Cited by Related Content   An iron( III )–catecholate complex of a facial tridentate ligand reacts with dioxygen in the presence of ammonium acetate–acetic acid buffer to cleave the aromatic C–C bond of 3,5-di- tert -butylcatechol regiospecifically resu...
Communication Copper-catalyzed direct oxysulfonylation of alkenes with dioxygen and sulfonylhydrazides leading to β-ketosulfones Wei Wei , a b      Chunli Liu , a b      Daoshan Yang , a b      Jiangwei Wen , a b    Jinmao You , a b c      Yourui Suo c  and     Hua Wang * a b    Show Affiliations Chem. Commun. , 2013, Advance Article DOI:  10.1039/C3CC45803B Received 30 Jul 2013, Accepted 10 Sep 2013 First published online 10 Sep 2013 | | Share on citeulike | Share on facebook | Share on twitter | | More PDF Rich HTML    Send PDF to Kindle Download Citation BibTex   EndNote   MEDLINE   ProCite   ReferenceManager   RefWorks   RIS   Request Permissions Abstract Cited by Related Content The first copper-catalyzed oxysulfonylation reaction of alkenes with ...