Organometallic Ruthenium and Iridium Transfer-Hydrogenation Catalysts Using Coenzyme NADH as a Cofactor
Artificial enzymes: Half‐sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N‐chelated ligands can use NADH as a source of hydride for the reduction of ketones (see picture). Moreover, cyclopentadienyl phenanthroline iridium(III) derivatives at micromolar concentra...
Saved in:
| Published in | Angewandte Chemie International Edition Vol. 51; no. 16; pp. 3897 - 3900 |
|---|---|
| Main Authors | , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Weinheim
WILEY-VCH Verlag
16.04.2012
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
| Edition | International ed. in English |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1433-7851 1521-3773 1521-3773 |
| DOI | 10.1002/anie.201108175 |
Cover
Loading…
| Abstract | Artificial enzymes: Half‐sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N‐chelated ligands can use NADH as a source of hydride for the reduction of ketones (see picture). Moreover, cyclopentadienyl phenanthroline iridium(III) derivatives at micromolar concentrations are robust catalysts for the production of H2 from NADH in water and can raise the NAD+/NADH ratio in cancer cells. |
|---|---|
| AbstractList | Artificial enzymes: half-sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N-chelated ligands can use NADH as a source of hydride for the reduction of ketones. Moreover, cyclopentadienyl phenanthroline iridium(III) derivatives at micromolar concentrations are robust catalysts for the production of H(2) from NADH in water and can raise the NAD(+)/NADH ratio in cancer cells. Artificial enzymes: half-sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N-chelated ligands can use NADH as a source of hydride for the reduction of ketones. Moreover, cyclopentadienyl phenanthroline iridium(III) derivatives at micromolar concentrations are robust catalysts for the production of H(2) from NADH in water and can raise the NAD(+)/NADH ratio in cancer cells.Artificial enzymes: half-sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N-chelated ligands can use NADH as a source of hydride for the reduction of ketones. Moreover, cyclopentadienyl phenanthroline iridium(III) derivatives at micromolar concentrations are robust catalysts for the production of H(2) from NADH in water and can raise the NAD(+)/NADH ratio in cancer cells. Artificial enzymes: Half‐sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N‐chelated ligands can use NADH as a source of hydride for the reduction of ketones (see picture). Moreover, cyclopentadienyl phenanthroline iridium(III) derivatives at micromolar concentrations are robust catalysts for the production of H2 from NADH in water and can raise the NAD+/NADH ratio in cancer cells. Artificial enzymes: Half-sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N-chelated ligands can use NADH as a source of hydride for the reduction of ketones (see picture). Moreover, cyclopentadienyl phenanthroline iridium(III) derivatives at micromolar concentrations are robust catalysts for the production of H sub(2) from NADH in water and can raise the NAD super(+)/NADH ratio in cancer cells. |
| Author | Liu, Zhe Habtemariam, Abraha Pizarro, Ana M. Qamar, Bushra Sadler, Peter J. Betanzos-Lara, Soledad |
| Author_xml | – sequence: 1 givenname: Soledad surname: Betanzos-Lara fullname: Betanzos-Lara, Soledad organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 2 givenname: Zhe surname: Liu fullname: Liu, Zhe organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 3 givenname: Abraha surname: Habtemariam fullname: Habtemariam, Abraha organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 4 givenname: Ana M. surname: Pizarro fullname: Pizarro, Ana M. organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 5 givenname: Bushra surname: Qamar fullname: Qamar, Bushra organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) – sequence: 6 givenname: Peter J. surname: Sadler fullname: Sadler, Peter J. email: p.j.sadler@warwick.ac.uk organization: Department of Chemistry, University of Warwick, Coventry, CV4 7AL (UK) |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22415924$$D View this record in MEDLINE/PubMed |
| BookMark | eNqFkU1r3DAQhkVJab567bEYekgv3urDsq3jsk2zS4IDISFHobVmt0ptKZVkUvfXV-4moQTa6qJheJ6BeecQ7VlnAaF3BM8IxvSTsgZmFBOCa1LxV-iAcEpyVlVsL9UFY3lVc7KPDkO4S3xd4_IN2qe0IFzQ4gBtL_1WWddDVF1n2uxqiF_BmqHPlNXZyhs91dde2bABny9H7d0WrIrG2WyhkjWGGLKbYOw2WziwP8cesmb-eZmpkKnU2qg2On-MXm9UF-Dt43-Ebr6cXi-W-cXl2Woxv8hbjgXPK75mmrcMEwykhUJTvhZYl3h6tKgqUKkGjTUwrGrC06Y1FYrWYl2KomBH6GQ399677wOEKHsTWug6ZcENQQrBBKGYi0R-_CdJqpQq4QWjCf3wAr1zg7dpD0k4Kcu6xHSi3j9Sw7oHLe-96ZUf5VPYCSh2QOtdCB42sjXxd5LRK9NJguV0UzndVD7fNGmzF9rT5L8KYic8mA7G_9By3qxO_3TznWtChB_PrvLfZFmxhN82Z_K8OadN2klesV-BjsCW |
| CODEN | ACIEAY |
| CitedBy_id | crossref_primary_10_1021_jacs_7b03872 crossref_primary_10_1002_cctc_201601307 crossref_primary_10_1021_acs_jmedchem_5b00288 crossref_primary_10_1021_jacs_3c10369 crossref_primary_10_1021_ic400835n crossref_primary_10_1016_j_electacta_2023_142954 crossref_primary_10_1021_cb400070a crossref_primary_10_1021_acsbiomaterials_3c00909 crossref_primary_10_3184_003685014X13898980185076 crossref_primary_10_1039_D2DT01055K crossref_primary_10_1016_j_cclet_2021_11_017 crossref_primary_10_1002_aoc_5053 crossref_primary_10_3390_inorganics9040026 crossref_primary_10_1021_acs_inorgchem_7b01959 crossref_primary_10_1039_C9QI01161G crossref_primary_10_1016_j_jorganchem_2014_12_041 crossref_primary_10_1016_j_cbpa_2015_01_024 crossref_primary_10_1039_D3DT01696J crossref_primary_10_1002_cctc_201200834 crossref_primary_10_1039_C8NJ03360A crossref_primary_10_1007_s00775_018_1578_0 crossref_primary_10_1021_acscatal_9b00513 crossref_primary_10_1021_acs_inorgchem_2c00059 crossref_primary_10_1021_acs_organomet_6b00179 crossref_primary_10_1002_cbic_201900268 crossref_primary_10_1039_C8DT02963F crossref_primary_10_1039_C8DT01858H crossref_primary_10_1021_ar400266c crossref_primary_10_1039_c3gc37129h crossref_primary_10_1039_C9QI01310E crossref_primary_10_1039_C9CS00917E crossref_primary_10_1021_acs_chemrev_5b00203 crossref_primary_10_1021_acs_inorgchem_0c03706 crossref_primary_10_1039_C7SC01778B crossref_primary_10_1002_ange_201311161 crossref_primary_10_1002_anie_201300747 crossref_primary_10_1039_C8CC09186B crossref_primary_10_1016_j_poly_2021_115379 crossref_primary_10_1021_acscatal_0c02261 crossref_primary_10_1016_j_jelechem_2020_113882 crossref_primary_10_1016_j_jinorgbio_2021_111622 crossref_primary_10_1021_acs_accounts_8b00618 crossref_primary_10_1021_acs_chemrev_1c00381 crossref_primary_10_1039_c3cc38977d crossref_primary_10_1016_j_ccr_2024_216139 crossref_primary_10_1002_anie_201702926 crossref_primary_10_1021_acscatal_3c02487 crossref_primary_10_1021_acs_inorgchem_8b00346 crossref_primary_10_1016_j_ejmech_2018_12_021 crossref_primary_10_1021_acsami_1c06381 crossref_primary_10_1039_C4DT03647F crossref_primary_10_1021_acs_inorgchem_8b00625 crossref_primary_10_1002_chem_202301603 crossref_primary_10_1039_D0DT03414B crossref_primary_10_1021_acs_inorgchem_5b02697 crossref_primary_10_1021_acs_chemrev_8b00493 crossref_primary_10_1039_C7DT00575J crossref_primary_10_1038_nchem_1498 crossref_primary_10_1039_C9DT02030F crossref_primary_10_1016_j_molcatb_2014_01_007 crossref_primary_10_1021_jm4004973 crossref_primary_10_1039_C2CC37832A crossref_primary_10_1039_D1FD00075F crossref_primary_10_1002_ange_201209484 crossref_primary_10_1002_asia_201800103 crossref_primary_10_3390_molecules25194540 crossref_primary_10_1039_D0SC04082G crossref_primary_10_1002_chem_202003927 crossref_primary_10_1021_acs_organomet_8b00402 crossref_primary_10_1021_jacs_6b02470 crossref_primary_10_1021_acs_inorgchem_8b01944 crossref_primary_10_1039_c3dt51275d crossref_primary_10_1039_D3CY01048A crossref_primary_10_1021_acs_chemrev_6b00168 crossref_primary_10_1021_acs_inorgchem_4c02314 crossref_primary_10_1039_D2QI00535B crossref_primary_10_1246_bcsj_20150189 crossref_primary_10_1016_j_ica_2021_120754 crossref_primary_10_1039_D0DT01547D crossref_primary_10_1002_advs_202404431 crossref_primary_10_1002_ange_201702926 crossref_primary_10_1039_C7DT02477K crossref_primary_10_1021_acs_inorgchem_6b01220 crossref_primary_10_1039_c2cc30678f crossref_primary_10_1039_D3DT02879H crossref_primary_10_1126_sciadv_abf6707 crossref_primary_10_1039_C3RA44131H crossref_primary_10_1002_anie_201209484 crossref_primary_10_1021_acscatal_6b00395 crossref_primary_10_1016_j_cbpa_2014_12_024 crossref_primary_10_1021_jacs_3c09735 crossref_primary_10_1039_C8DT00438B crossref_primary_10_2174_1570178618666210706112141 crossref_primary_10_1039_D4QI02472A crossref_primary_10_1021_acs_inorgchem_9b00853 crossref_primary_10_1039_D0CB00150C crossref_primary_10_1002_anie_201311161 crossref_primary_10_1002_chem_201701714 crossref_primary_10_1016_j_aca_2021_339126 crossref_primary_10_1021_acs_jmedchem_3c01156 crossref_primary_10_1039_D1SC01939B crossref_primary_10_1016_j_jinorgbio_2019_110983 crossref_primary_10_1098_rspb_2019_2377 crossref_primary_10_1016_j_ccr_2024_216306 crossref_primary_10_1039_C7CC08270C crossref_primary_10_1016_j_jorganchem_2024_123168 crossref_primary_10_1002_cmdc_201600638 crossref_primary_10_1016_j_jinorgbio_2024_112704 crossref_primary_10_1039_c3cs35466k crossref_primary_10_1039_C8DT03159B crossref_primary_10_1021_acsami_7b10258 crossref_primary_10_1016_j_ccr_2023_215230 crossref_primary_10_1002_chem_201800504 crossref_primary_10_1039_D0DT00627K crossref_primary_10_1016_j_jorganchem_2017_03_038 crossref_primary_10_1002_cssc_202200888 crossref_primary_10_1002_cssc_202101240 crossref_primary_10_1039_C7DT03265J crossref_primary_10_1016_j_ccr_2018_01_010 crossref_primary_10_1016_j_jinorgbio_2022_111820 crossref_primary_10_1021_acs_inorgchem_1c02250 crossref_primary_10_1038_ncomms7582 crossref_primary_10_1039_D2DT01085B crossref_primary_10_1039_C6DT01242F crossref_primary_10_1039_C8SC01142G crossref_primary_10_1002_anie_202403098 crossref_primary_10_1016_j_jcat_2023_115185 crossref_primary_10_1002_ejic_201600908 crossref_primary_10_1016_j_celbio_2025_100010 crossref_primary_10_1021_acs_jmedchem_4c00256 crossref_primary_10_3390_inorganics5030044 crossref_primary_10_1039_D0CC05450J crossref_primary_10_1016_j_jinorgbio_2015_10_008 crossref_primary_10_1016_j_jinorgbio_2021_111395 crossref_primary_10_3390_ijms232112779 crossref_primary_10_1002_ange_201300747 crossref_primary_10_1016_j_jorganchem_2016_10_018 crossref_primary_10_1002_cctc_201601633 crossref_primary_10_1016_j_dyepig_2018_08_006 crossref_primary_10_1002_ejic_201901055 crossref_primary_10_1039_D0DT01935F crossref_primary_10_1039_D1GC01256H crossref_primary_10_1002_aoc_4633 crossref_primary_10_1002_cmdc_202100297 crossref_primary_10_1007_s41061_016_0013_7 crossref_primary_10_1016_j_jinorgbio_2018_09_009 crossref_primary_10_1021_acs_inorgchem_5b01832 crossref_primary_10_1002_ange_202403098 crossref_primary_10_1007_s11244_013_0187_y crossref_primary_10_1021_acs_inorgchem_6b02474 crossref_primary_10_1002_chem_201806351 crossref_primary_10_1021_acs_organomet_5b00097 crossref_primary_10_1039_c3cc41143e crossref_primary_10_1002_cbic_202000511 crossref_primary_10_1002_hlca_202300001 crossref_primary_10_1021_acs_inorgchem_8b02161 crossref_primary_10_1016_j_jinorgbio_2024_112612 crossref_primary_10_1039_C6CC04604E crossref_primary_10_1039_c2sc20220d crossref_primary_10_1039_D0QI00846J |
| Cites_doi | 10.1021/ja00040a028 10.1021/jm2000932 10.1021/ja207785f 10.1021/om0300777 10.1038/nm1577 10.1016/j.tibs.2006.11.006 10.1002/anie.201102732 10.1039/c1ob05482a 10.1021/om00051a057 10.1016/S0955-0674(03)00006-1 10.1016/S0898-8838(09)00201-3 10.1002/anie.200500023 10.1039/B707077M 10.1002/ange.201102732 10.1039/c0cc02813d 10.1002/1521-3773(20020201)41:3<478::AID-ANIE478>3.0.CO;2-K 10.1016/j.cbpa.2007.05.013 10.1021/om00051a056 10.1021/ja00084a063 10.1007/s00775-006-0098-5 10.1021/om2005468 10.1071/CH10239 10.1002/(SICI)1521-3757(19990517)111:10<1524::AID-ANGE1524>3.0.CO;2-S 10.1002/1521-3757(20020201)114:3<496::AID-ANGE496>3.0.CO;2-Z 10.1016/j.ica.2006.02.037 10.1002/chem.201002399 10.1016/j.bbrc.2008.05.165 10.1021/ja206079e 10.1021/jm100020w 10.1002/ejic.200700505 10.1351/pac200173020209 10.1093/clinchem/24.5.828 10.1016/j.jorganchem.2007.04.048 10.1002/ange.200500023 10.1039/c1dt11007a 10.1038/nsb0396-213 10.1089/ars.2007.1672 10.1021/ic010562z 10.1021/ja0288237 10.1039/B916860P 10.1039/b508531b 10.1021/cr00078a002 10.1002/(SICI)1521-3773(19990517)38:10<1429::AID-ANIE1429>3.0.CO;2-Q |
| ContentType | Journal Article |
| Copyright | Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| Copyright_xml | – notice: Copyright © 2012 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim – notice: Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. – notice: Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
| DBID | BSCLL AAYXX CITATION CGR CUY CVF ECM EIF NPM 7TM K9. 7SR 8BQ 8FD JG9 7X8 |
| DOI | 10.1002/anie.201108175 |
| DatabaseName | Istex CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Nucleic Acids Abstracts ProQuest Health & Medical Complete (Alumni) Engineered Materials Abstracts METADEX Technology Research Database Materials Research Database MEDLINE - Academic |
| DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) ProQuest Health & Medical Complete (Alumni) Nucleic Acids Abstracts Materials Research Database Engineered Materials Abstracts Technology Research Database METADEX MEDLINE - Academic |
| DatabaseTitleList | ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic MEDLINE Materials Research Database |
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Chemistry |
| EISSN | 1521-3773 |
| Edition | International ed. in English |
| EndPage | 3900 |
| ExternalDocumentID | 3277256891 22415924 10_1002_anie_201108175 ANIE201108175 ark_67375_WNG_KNK2N159_R |
| Genre | shortCommunication Research Support, Non-U.S. Gov't Journal Article |
| GrantInformation_xml | – fundername: WPRS – fundername: EPSRC – fundername: AWM – fundername: ORSAS – fundername: ERC – fundername: CONACyT Mexico – fundername: ERDF |
| GroupedDBID | --- -DZ -~X .3N .GA .Y3 05W 0R~ 10A 1L6 1OB 1OC 1ZS 23M 31~ 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5RE 5VS 66C 6TJ 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A03 AAESR AAEVG AAHHS AANLZ AAONW AASGY AAXRX AAZKR ABCQN ABCUV ABEML ABIJN ABLJU ABPPZ ABPVW ACAHQ ACBWZ ACCFJ ACCZN ACFBH ACGFS ACIWK ACNCT ACPOU ACPRK ACSCC ACXBN ACXQS ADBBV ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AEQDE AEUQT AEUYR AFBPY AFFNX AFFPM AFGKR AFPWT AFRAH AFZJQ AHBTC AHMBA AITYG AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ATUGU AUFTA AZBYB AZFZN AZVAB B-7 BAFTC BDRZF BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BSCLL BTSUX BY8 CS3 D-E D-F D0L DCZOG DPXWK DR1 DR2 DRFUL DRSTM EBS EJD F00 F01 F04 F5P FEDTE G-S G.N GNP GODZA H.T H.X HBH HF~ HGLYW HHY HHZ HVGLF HZ~ IX1 J0M JPC KQQ LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES M53 MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG P2P P2W P2X P4D PQQKQ Q.N Q11 QB0 QRW R.K RNS ROL RWI RX1 RYL SUPJJ TN5 UB1 UPT V2E VQA W8V W99 WBFHL WBKPD WH7 WIB WIH WIK WJL WOHZO WQJ WRC WXSBR WYISQ XG1 XPP XSW XV2 YZZ ZZTAW ~IA ~KM ~WT AAHQN AAMNL AANHP AAYCA ACRPL ACYXJ ADNMO AFWVQ ALVPJ AAYXX ABDBF ABJNI AETEA AEYWJ AGQPQ AGYGG CITATION CGR CUY CVF ECM EIF NPM 7TM K9. 7SR 8BQ 8FD JG9 7X8 |
| ID | FETCH-LOGICAL-c5095-75b3d5c3010e1ce4d25b90d6000002477ea600ed0de30a815377829a289b69443 |
| IEDL.DBID | DR2 |
| ISSN | 1433-7851 1521-3773 |
| IngestDate | Fri Jul 11 10:11:21 EDT 2025 Fri Jul 11 15:08:42 EDT 2025 Sun Jul 13 04:37:03 EDT 2025 Thu Apr 03 07:09:24 EDT 2025 Tue Jul 01 02:52:56 EDT 2025 Thu Apr 24 23:00:22 EDT 2025 Wed Jan 22 17:12:34 EST 2025 Wed Oct 30 09:52:24 EDT 2024 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 16 |
| Language | English |
| License | http://onlinelibrary.wiley.com/termsAndConditions#vor Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-c5095-75b3d5c3010e1ce4d25b90d6000002477ea600ed0de30a815377829a289b69443 |
| Notes | WPRS CONACyT Mexico ArticleID:ANIE201108175 We thank the WPRS and the ORSAS (S.B.-L. and Z.L.), and the CONACyT Mexico (S.B-L.) for research scholarships, the EPSRC, the ERC (BIOINCMED), the ERDF, and the AWM (Science City) for funding. Dr. Ivan Prokes, Dr. Lijiang Song, and Mr Philip Aston (University of Warwick) are acknowledged for assistance with the NMR and MS instruments, respectively, Prof. Colin Murrell and Dr. Andrew Crombie are thanked for assistance with the gas chromatograph, and Dr. Ying Fu and Dr. Maria Romero Castro are thanked for helpful discussions. ERC AWM EPSRC ark:/67375/WNG-KNK2N159-R ORSAS ERDF istex:E0A09C6928D77CD1FD806A80D883BB4153646BA0 The first two authors are equal first authors. We thank the WPRS and the ORSAS (S.B.‐L. and Z.L.), and the CONACyT Mexico (S.B‐L.) for research scholarships, the EPSRC, the ERC (BIOINCMED), the ERDF, and the AWM (Science City) for funding. Dr. Ivan Prokes, Dr. Lijiang Song, and Mr Philip Aston (University of Warwick) are acknowledged for assistance with the NMR and MS instruments, respectively, Prof. Colin Murrell and Dr. Andrew Crombie are thanked for assistance with the gas chromatograph, and Dr. Ying Fu and Dr. Maria Romero Castro are thanked for helpful discussions. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
| PMID | 22415924 |
| PQID | 1516686022 |
| PQPubID | 946352 |
| PageCount | 4 |
| ParticipantIDs | proquest_miscellaneous_993912059 proquest_miscellaneous_1701115432 proquest_journals_1516686022 pubmed_primary_22415924 crossref_citationtrail_10_1002_anie_201108175 crossref_primary_10_1002_anie_201108175 wiley_primary_10_1002_anie_201108175_ANIE201108175 istex_primary_ark_67375_WNG_KNK2N159_R |
| ProviderPackageCode | CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | April 16, 2012 |
| PublicationDateYYYYMMDD | 2012-04-16 |
| PublicationDate_xml | – month: 04 year: 2012 text: April 16, 2012 day: 16 |
| PublicationDecade | 2010 |
| PublicationPlace | Weinheim |
| PublicationPlace_xml | – name: Weinheim – name: Germany |
| PublicationTitle | Angewandte Chemie International Edition |
| PublicationTitleAlternate | Angew. Chem. Int. Ed |
| PublicationYear | 2012 |
| Publisher | WILEY-VCH Verlag WILEY‐VCH Verlag Wiley Subscription Services, Inc |
| Publisher_xml | – name: WILEY-VCH Verlag – name: WILEY‐VCH Verlag – name: Wiley Subscription Services, Inc |
| References | W. Ying, Antioxid. Redox Signaling 2008, 10, 179-206 R. H. Fish, G. Jaouen, Organometallics 2003, 22, 2166-2177 Y. Yamada, T. Miyahigashi, H. Kotani, K. Ohkubo, S. Fukuzumi, J. Am. Chem. Soc. 2011, 133, 16136-16145. G. Gasser, I. Ott, N. Metzler-Nolte, J. Med. Chem. 2011, 54, 3-25 H. Vázquez-Villa, S. Reber, M. A. Ariger, E. M. Carreira, Angew. Chem. 2011, 123, 9141-9143 W. D. Jones, V. L. Kuykendall, A. D. Selmeczy, Organometallics 1991, 10, 1577-1586. E. Steckhan, S. Herrmann, R. Ruppert, E. Dietz, M. Frede, E. Spika, Organometallics 1991, 10, 1568-1577 P. Belenky, K. L. Bogan, C. Brenner, Trends Biochem. Sci. 2007, 32, 12-19 X. Wu, X. Li, F. King, J. Xiao, Angew. Chem. 2005, 117, 3473-3477 J. Halpern, Pure Appl. Chem. 2001, 73, 209-220 H. C. Lo, C. Leiva, O. Buriez, J. B. Kerr, M. M. Olmstead, R. H. Fish, Inorg. Chem. 2001, 40, 6705-6716. Medicinal Organometallic Chemistry (Topics in Organometallic Chemistry), Vol. 32, 1 st ed. (Eds.: G. Jaouen, N. Metzler-Nolte), Springer, Heidelberg, 2010 G. Jaouen, Bioorganometallics: Biomolecules, Labeling, Medicine, Wiley-VCH, Weinheim, 2006 J. P. Collman, P. S. Wagenknecht, N. S. Lewis, J. Am. Chem. Soc. 1992, 114, 5665-5673 Y. Maenaka, T. Suenobu, S. Fukuzumi, J. Am. Chem. Soc. 2012, 134, 367-374. E. Meggers, Curr. Opin. Chem. Biol. 2007, 11, 287-292 H. C. Lo, R. H. Fish, Angew. Chem. 2002, 114, 496-499 Y. Yan, M. Melchart, A. Habtemariam, A. Peacock, P. Sadler, J. Biol. Inorg. Chem. 2006, 11, 483-488 P. C. A. Bruijnincx, P. J. Sadler in Advances in Inorganic Chemistry, Vol. 61 (Eds.: E. Rudi van, C. D. Hubbard), Academic Press, New York, 2009, pp. 1-62 Interestingly the compatibility of simultaneous Ir-catalyzed oxidation (of alcohols) with ADH-catalyzed reduction has been demonstrated: F. G. Mutti, A. Orthaber, J. H. Schrittwieser, J. G. d. Vries, R. Pietschnig, W. Kroutil, Chem. Commun. 2010, 46, 8046-8048. Z. Liu, A. Habtemariam, A. M. Pizarro, G. J. Clarkson, P. J. Sadler, Organometallics 2011, 30, 4702-4710. R. H. Fish, Aust. J. Chem. 2010, 63, 1505-1513. H. C. Lo, O. Buriez, J. B. Kerr, R. H. Fish, Angew. Chem. 1999, 111, 1524-1527 J. P. Collman, Nat. Struct. Biol. 1996, 3, 213-217. S.-J. Lin, L. Guarente, Curr. Opin. Cell Biol. 2003, 15, 241-246. P. Haquette, B. Talbi, L. Barilleau, N. Madern, C. Fosse, M. Salmain, Org. Biomol. Chem. 2011, 9, 5720-5727. H. Kotani, R. Hanazaki, K. Ohkubo, Y. Yamada, S. Fukuzumi, Chem. Eur. J. 2011, 17, 2777-2785 P. Štěpnička, J. Ludvík, J. Canivet, G. Süss-Fink, Inorg. Chim. Acta 2006, 359, 2369-2374 K. Hayashida, M. Sano, I. Ohsawa, K. Shinmura, K. Tamaki, K. Kimura, J. Endo, T. Katayama, A. Kawamura, S. Kohsaka, S. Makino, S. Ohta, S. Ogawa, K. Fukuda, Biochem. Biophys. Res. Commun. 2008, 373, 30-35. Z. Liu, A. Habtemariam, A. M. Pizarro, S. A. Fletcher, A. Kisova, O. Vrana, L. Salassa, P. C. A. Bruijnincx, G. J. Clarkson, V. Brabec, P. J. Sadler, J. Med. Chem. 2011, 54, 3011-3026 J. Canivet, G. Süss-Fink, P. Štěpnička, Eur. J. Inorg. Chem. 2007, 4736-4742 J. M. O'Connor, C. P. Casey, Chem. Rev. 1987, 87, 307-318. S. Buhl, K. Jackson, Clin. Chem. 1978, 24, 828-831. Angew. Chem. Int. Ed. 2002, 41, 478-481. C. G. Hartinger, P. J. Dyson, Chem. Soc. Rev. 2009, 38, 391-401 G. S. Smith, B. Therrien, Dalton Trans. 2011, 40, 10793-10800 R. T. Hembre, S. McQueen, J. Am. Chem. Soc. 1994, 116, 2141-2142 T. Abura, S. Ogo, Y. Watanabe, S. Fukuzumi, J. Am. Chem. Soc. 2003, 125, 4149-4154. I. Ohsawa, M. Ishikawa, K. Takahashi, M. Watanabe, K. Nishimaki, K. Yamagata, K.-i. Katsura, Y. Katayama, S. Asoh, S. Ohta, Nat. Med. 2007, 13, 688-694 P. Govindaswamy, J. Canivet, B. Therrien, G. Süss-Fink, P. Stepnicka, J. Ludvík, J. Organomet. Chem. 2007, 692, 3664-3675. Angew. Chem. Int. Ed. 1999, 38, 1429-1432 Y. K. Yan, M. Melchart, A. Habtemariam, P. J. Sadler, Chem. Commun. 2005, 4764-4776 Angew. Chem. Int. Ed. 2011, 50, 8979-8981. G. Süss-Fink, Dalton Trans. 2010, 39, 1673-1688 Angew. Chem. Int. Ed. 2005, 44, 3407-3411 1994; 116 2002 2002; 114 41 2011 2010 1991; 10 2010; 39 2006; 11 1999 1999; 111 38 2011; 40 2009 2011; 30 2007 2003; 15 2006 2011; 54 2005 2008; 10 2011 2011; 123 50 2011; 17 2007; 32 2007; 11 2006; 359 2010; 63 2001; 40 2007; 13 2011; 133 2011; 9 1987; 87 2012; 134 2010; 46 1992; 114 2007; 692 1978; 24 2003; 125 1996; 3 2008; 373 2001; 73 2009; 38 2003; 22 2005 2005; 117 44 e_1_2_2_24_2 e_1_2_2_47_2 e_1_2_2_4_2 Jaouen G. (e_1_2_2_6_2) 2006 e_1_2_2_22_2 e_1_2_2_49_2 e_1_2_2_20_3 e_1_2_2_20_2 e_1_2_2_2_2 e_1_2_2_41_2 e_1_2_2_28_2 e_1_2_2_43_2 e_1_2_2_26_2 e_1_2_2_45_2 e_1_2_2_24_3 e_1_2_2_13_2 e_1_2_2_36_2 e_1_2_2_11_2 e_1_2_2_38_2 e_1_2_2_51_2 e_1_2_2_19_2 e_1_2_2_30_2 e_1_2_2_51_3 e_1_2_2_17_2 e_1_2_2_32_2 e_1_2_2_15_2 e_1_2_2_34_2 e_1_2_2_3_2 e_1_2_2_23_2 e_1_2_2_48_2 e_1_2_2_5_2 e_1_2_2_21_2 e_1_2_2_1_2 e_1_2_2_40_2 (e_1_2_2_8_2) 2010 e_1_2_2_29_2 e_1_2_2_42_2 e_1_2_2_7_2 e_1_2_2_27_2 e_1_2_2_44_2 e_1_2_2_9_2 e_1_2_2_25_2 e_1_2_2_46_2 e_1_2_2_12_2 e_1_2_2_37_2 e_1_2_2_10_2 e_1_2_2_39_2 e_1_2_2_50_2 e_1_2_2_52_3 e_1_2_2_18_2 e_1_2_2_31_2 e_1_2_2_52_2 e_1_2_2_16_2 e_1_2_2_33_2 e_1_2_2_14_2 e_1_2_2_35_2 |
| References_xml | – reference: J. P. Collman, P. S. Wagenknecht, N. S. Lewis, J. Am. Chem. Soc. 1992, 114, 5665-5673; – reference: Y. Yan, M. Melchart, A. Habtemariam, A. Peacock, P. Sadler, J. Biol. Inorg. Chem. 2006, 11, 483-488; – reference: E. Meggers, Curr. Opin. Chem. Biol. 2007, 11, 287-292; – reference: Angew. Chem. Int. Ed. 2005, 44, 3407-3411; – reference: J. Canivet, G. Süss-Fink, P. Štěpnička, Eur. J. Inorg. Chem. 2007, 4736-4742; – reference: Z. Liu, A. Habtemariam, A. M. Pizarro, S. A. Fletcher, A. Kisova, O. Vrana, L. Salassa, P. C. A. Bruijnincx, G. J. Clarkson, V. Brabec, P. J. Sadler, J. Med. Chem. 2011, 54, 3011-3026; – reference: T. Abura, S. Ogo, Y. Watanabe, S. Fukuzumi, J. Am. Chem. Soc. 2003, 125, 4149-4154. – reference: X. Wu, X. Li, F. King, J. Xiao, Angew. Chem. 2005, 117, 3473-3477; – reference: H. Vázquez-Villa, S. Reber, M. A. Ariger, E. M. Carreira, Angew. Chem. 2011, 123, 9141-9143; – reference: Angew. Chem. Int. Ed. 2002, 41, 478-481. – reference: Z. Liu, A. Habtemariam, A. M. Pizarro, G. J. Clarkson, P. J. Sadler, Organometallics 2011, 30, 4702-4710. – reference: Angew. Chem. Int. Ed. 1999, 38, 1429-1432; – reference: J. Halpern, Pure Appl. Chem. 2001, 73, 209-220; – reference: R. T. Hembre, S. McQueen, J. Am. Chem. Soc. 1994, 116, 2141-2142; – reference: G. Gasser, I. Ott, N. Metzler-Nolte, J. Med. Chem. 2011, 54, 3-25; – reference: P. Govindaswamy, J. Canivet, B. Therrien, G. Süss-Fink, P. Stepnicka, J. Ludvík, J. Organomet. Chem. 2007, 692, 3664-3675. – reference: S. Buhl, K. Jackson, Clin. Chem. 1978, 24, 828-831. – reference: E. Steckhan, S. Herrmann, R. Ruppert, E. Dietz, M. Frede, E. Spika, Organometallics 1991, 10, 1568-1577; – reference: R. H. Fish, G. Jaouen, Organometallics 2003, 22, 2166-2177; – reference: W. Ying, Antioxid. Redox Signaling 2008, 10, 179-206; – reference: Medicinal Organometallic Chemistry (Topics in Organometallic Chemistry), Vol. 32, 1 st ed. (Eds.: G. Jaouen, N. Metzler-Nolte), Springer, Heidelberg, 2010; – reference: Angew. Chem. Int. Ed. 2011, 50, 8979-8981. – reference: W. D. Jones, V. L. Kuykendall, A. D. Selmeczy, Organometallics 1991, 10, 1577-1586. – reference: H. C. Lo, C. Leiva, O. Buriez, J. B. Kerr, M. M. Olmstead, R. H. Fish, Inorg. Chem. 2001, 40, 6705-6716. – reference: I. Ohsawa, M. Ishikawa, K. Takahashi, M. Watanabe, K. Nishimaki, K. Yamagata, K.-i. Katsura, Y. Katayama, S. Asoh, S. Ohta, Nat. Med. 2007, 13, 688-694; – reference: H. C. Lo, O. Buriez, J. B. Kerr, R. H. Fish, Angew. Chem. 1999, 111, 1524-1527; – reference: Y. K. Yan, M. Melchart, A. Habtemariam, P. J. Sadler, Chem. Commun. 2005, 4764-4776; – reference: Interestingly the compatibility of simultaneous Ir-catalyzed oxidation (of alcohols) with ADH-catalyzed reduction has been demonstrated: F. G. Mutti, A. Orthaber, J. H. Schrittwieser, J. G. d. Vries, R. Pietschnig, W. Kroutil, Chem. Commun. 2010, 46, 8046-8048. – reference: P. Haquette, B. Talbi, L. Barilleau, N. Madern, C. Fosse, M. Salmain, Org. Biomol. Chem. 2011, 9, 5720-5727. – reference: C. G. Hartinger, P. J. Dyson, Chem. Soc. Rev. 2009, 38, 391-401; – reference: Y. Yamada, T. Miyahigashi, H. Kotani, K. Ohkubo, S. Fukuzumi, J. Am. Chem. Soc. 2011, 133, 16136-16145. – reference: H. C. Lo, R. H. Fish, Angew. Chem. 2002, 114, 496-499; – reference: G. Jaouen, Bioorganometallics: Biomolecules, Labeling, Medicine, Wiley-VCH, Weinheim, 2006; – reference: G. S. Smith, B. Therrien, Dalton Trans. 2011, 40, 10793-10800; – reference: J. M. O'Connor, C. P. Casey, Chem. Rev. 1987, 87, 307-318. – reference: G. Süss-Fink, Dalton Trans. 2010, 39, 1673-1688; – reference: P. C. A. Bruijnincx, P. J. Sadler in Advances in Inorganic Chemistry, Vol. 61 (Eds.: E. Rudi van, C. D. Hubbard), Academic Press, New York, 2009, pp. 1-62; – reference: K. Hayashida, M. Sano, I. Ohsawa, K. Shinmura, K. Tamaki, K. Kimura, J. Endo, T. Katayama, A. Kawamura, S. Kohsaka, S. Makino, S. Ohta, S. Ogawa, K. Fukuda, Biochem. Biophys. Res. Commun. 2008, 373, 30-35. – reference: R. H. Fish, Aust. J. Chem. 2010, 63, 1505-1513. – reference: J. P. Collman, Nat. Struct. Biol. 1996, 3, 213-217. – reference: Y. Maenaka, T. Suenobu, S. Fukuzumi, J. Am. Chem. Soc. 2012, 134, 367-374. – reference: P. Belenky, K. L. Bogan, C. Brenner, Trends Biochem. Sci. 2007, 32, 12-19; – reference: P. Štěpnička, J. Ludvík, J. Canivet, G. Süss-Fink, Inorg. Chim. Acta 2006, 359, 2369-2374; – reference: H. Kotani, R. Hanazaki, K. Ohkubo, Y. Yamada, S. Fukuzumi, Chem. Eur. J. 2011, 17, 2777-2785; – reference: S.-J. Lin, L. Guarente, Curr. Opin. Cell Biol. 2003, 15, 241-246. – volume: 9 start-page: 5720 year: 2011 end-page: 5727 publication-title: Org. Biomol. Chem. – year: 2011 – volume: 46 start-page: 8046 year: 2010 end-page: 8048 publication-title: Chem. Commun. – start-page: 4736 year: 2007 end-page: 4742 publication-title: Eur. J. Inorg. Chem. – volume: 39 start-page: 1673 year: 2010 end-page: 1688 publication-title: Dalton Trans. – volume: 111 38 start-page: 1524 1429 year: 1999 1999 end-page: 1527 1432 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 15 start-page: 241 year: 2003 end-page: 246 publication-title: Curr. Opin. Cell Biol. – volume: 13 start-page: 688 year: 2007 end-page: 694 publication-title: Nat. Med. – volume: 134 start-page: 367 year: 2012 end-page: 374 publication-title: J. Am. Chem. Soc. – volume: 10 start-page: 179 year: 2008 end-page: 206 publication-title: Antioxid. Redox Signaling – volume: 114 start-page: 5665 year: 1992 end-page: 5673 publication-title: J. Am. Chem. Soc. – volume: 54 start-page: 3011 year: 2011 end-page: 3026 publication-title: J. Med. Chem. – volume: 692 start-page: 3664 year: 2007 end-page: 3675 publication-title: J. Organomet. Chem. – volume: 10 start-page: 1568 year: 1991 end-page: 1577 publication-title: Organometallics – volume: 32 start-page: 12 year: 2007 end-page: 19 publication-title: Trends Biochem. Sci. – volume: 38 start-page: 391 year: 2009 end-page: 401 publication-title: Chem. Soc. Rev. – volume: 63 start-page: 1505 year: 2010 end-page: 1513 publication-title: Aust. J. Chem. – volume: 3 start-page: 213 year: 1996 end-page: 217 publication-title: Nat. Struct. Biol. – volume: 40 start-page: 10793 year: 2011 end-page: 10800 publication-title: Dalton Trans. – volume: 117 44 start-page: 3473 3407 year: 2005 2005 end-page: 3477 3411 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 22 start-page: 2166 year: 2003 end-page: 2177 publication-title: Organometallics – year: 2010 – volume: 24 start-page: 828 year: 1978 end-page: 831 publication-title: Clin. Chem. – volume: 54 start-page: 3 year: 2011 end-page: 25 publication-title: J. Med. Chem. – start-page: 1 year: 2009 end-page: 62 – volume: 30 start-page: 4702 year: 2011 end-page: 4710 publication-title: Organometallics – volume: 123 50 start-page: 9141 8979 year: 2011 2011 end-page: 9143 8981 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 40 start-page: 6705 year: 2001 end-page: 6716 publication-title: Inorg. Chem. – volume: 10 start-page: 1577 year: 1991 end-page: 1586 publication-title: Organometallics – volume: 73 start-page: 209 year: 2001 end-page: 220 publication-title: Pure Appl. Chem. – volume: 17 start-page: 2777 year: 2011 end-page: 2785 publication-title: Chem. Eur. J. – volume: 133 start-page: 16136 year: 2011 end-page: 16145 publication-title: J. Am. Chem. Soc. – start-page: 4764 year: 2005 end-page: 4776 publication-title: Chem. Commun. – volume: 11 start-page: 483 year: 2006 end-page: 488 publication-title: J. Biol. Inorg. Chem. – year: 2006 – volume: 373 start-page: 30 year: 2008 end-page: 35 publication-title: Biochem. Biophys. Res. Commun. – volume: 11 start-page: 287 year: 2007 end-page: 292 publication-title: Curr. Opin. Chem. Biol. – volume: 116 start-page: 2141 year: 1994 end-page: 2142 publication-title: J. Am. Chem. Soc. – volume: 114 41 start-page: 496 478 year: 2002 2002 end-page: 499 481 publication-title: Angew. Chem. Angew. Chem. Int. Ed. – volume: 359 start-page: 2369 year: 2006 end-page: 2374 publication-title: Inorg. Chim. Acta – volume: 125 start-page: 4149 year: 2003 end-page: 4154 publication-title: J. Am. Chem. Soc. – volume: 87 start-page: 307 year: 1987 end-page: 318 publication-title: Chem. Rev. – ident: e_1_2_2_15_2 doi: 10.1021/ja00040a028 – ident: e_1_2_2_44_2 doi: 10.1021/jm2000932 – ident: e_1_2_2_49_2 doi: 10.1021/ja207785f – ident: e_1_2_2_3_2 doi: 10.1021/om0300777 – ident: e_1_2_2_30_2 – ident: e_1_2_2_47_2 doi: 10.1038/nm1577 – volume-title: Bioorganometallics: Biomolecules, Labeling, Medicine year: 2006 ident: e_1_2_2_6_2 – ident: e_1_2_2_22_2 – ident: e_1_2_2_28_2 doi: 10.1016/j.tibs.2006.11.006 – ident: e_1_2_2_52_3 doi: 10.1002/anie.201102732 – ident: e_1_2_2_13_2 – ident: e_1_2_2_21_2 doi: 10.1039/c1ob05482a – ident: e_1_2_2_40_2 doi: 10.1021/om00051a057 – ident: e_1_2_2_29_2 doi: 10.1016/S0955-0674(03)00006-1 – ident: e_1_2_2_43_2 doi: 10.1016/S0898-8838(09)00201-3 – ident: e_1_2_2_51_3 doi: 10.1002/anie.200500023 – ident: e_1_2_2_7_2 doi: 10.1039/B707077M – ident: e_1_2_2_46_2 – ident: e_1_2_2_52_2 doi: 10.1002/ange.201102732 – ident: e_1_2_2_36_2 doi: 10.1039/c0cc02813d – ident: e_1_2_2_24_3 doi: 10.1002/1521-3773(20020201)41:3<478::AID-ANIE478>3.0.CO;2-K – ident: e_1_2_2_5_2 doi: 10.1016/j.cbpa.2007.05.013 – ident: e_1_2_2_23_2 doi: 10.1021/om00051a056 – ident: e_1_2_2_14_2 doi: 10.1021/ja00084a063 – ident: e_1_2_2_18_2 doi: 10.1007/s00775-006-0098-5 – ident: e_1_2_2_45_2 doi: 10.1021/om2005468 – ident: e_1_2_2_12_2 doi: 10.1071/CH10239 – ident: e_1_2_2_20_2 doi: 10.1002/(SICI)1521-3757(19990517)111:10<1524::AID-ANGE1524>3.0.CO;2-S – ident: e_1_2_2_17_2 – ident: e_1_2_2_24_2 doi: 10.1002/1521-3757(20020201)114:3<496::AID-ANGE496>3.0.CO;2-Z – ident: e_1_2_2_32_2 doi: 10.1016/j.ica.2006.02.037 – ident: e_1_2_2_38_2 doi: 10.1002/chem.201002399 – ident: e_1_2_2_48_2 doi: 10.1016/j.bbrc.2008.05.165 – ident: e_1_2_2_39_2 doi: 10.1021/ja206079e – ident: e_1_2_2_9_2 doi: 10.1021/jm100020w – ident: e_1_2_2_19_2 doi: 10.1002/ejic.200700505 – ident: e_1_2_2_2_2 doi: 10.1351/pac200173020209 – ident: e_1_2_2_34_2 doi: 10.1093/clinchem/24.5.828 – ident: e_1_2_2_33_2 doi: 10.1016/j.jorganchem.2007.04.048 – ident: e_1_2_2_51_2 doi: 10.1002/ange.200500023 – ident: e_1_2_2_1_2 – volume-title: Medicinal Organometallic Chemistry (Topics in Organometallic Chemistry), Vol. 32 year: 2010 ident: e_1_2_2_8_2 – ident: e_1_2_2_10_2 doi: 10.1039/c1dt11007a – ident: e_1_2_2_16_2 doi: 10.1038/nsb0396-213 – ident: e_1_2_2_37_2 – ident: e_1_2_2_31_2 – ident: e_1_2_2_27_2 doi: 10.1089/ars.2007.1672 – ident: e_1_2_2_25_2 doi: 10.1021/ic010562z – ident: e_1_2_2_35_2 doi: 10.1021/ja0288237 – ident: e_1_2_2_11_2 doi: 10.1039/B916860P – ident: e_1_2_2_42_2 – ident: e_1_2_2_4_2 doi: 10.1039/b508531b – ident: e_1_2_2_41_2 doi: 10.1021/cr00078a002 – ident: e_1_2_2_20_3 doi: 10.1002/(SICI)1521-3773(19990517)38:10<1429::AID-ANIE1429>3.0.CO;2-Q – ident: e_1_2_2_50_2 – ident: e_1_2_2_26_2 |
| SSID | ssj0028806 |
| Score | 2.4666626 |
| Snippet | Artificial enzymes: Half‐sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N‐chelated ligands can use NADH as a source of... Artificial enzymes: half-sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N-chelated ligands can use NADH as a source of... Artificial enzymes: Half-sandwich arene ruthenium(II) and cyclopentadienyl iridium(III) complexes containing N,N-chelated ligands can use NADH as a source of... |
| SourceID | proquest pubmed crossref wiley istex |
| SourceType | Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 3897 |
| SubjectTerms | arenes bio-organometallics Catalysis Catalysts Cell Line, Tumor Coordination Complexes - chemistry Derivatives Humans hydride transfer Hydrides Hydrogenation Iridium Iridium - chemistry Ketones Ketones - chemistry Ligands Metalorganic compounds NAD - chemistry NADH Oxidation-Reduction Ruthenium Ruthenium - chemistry Water - chemistry |
| Title | Organometallic Ruthenium and Iridium Transfer-Hydrogenation Catalysts Using Coenzyme NADH as a Cofactor |
| URI | https://api.istex.fr/ark:/67375/WNG-KNK2N159-R/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201108175 https://www.ncbi.nlm.nih.gov/pubmed/22415924 https://www.proquest.com/docview/1516686022 https://www.proquest.com/docview/1701115432 https://www.proquest.com/docview/993912059 |
| Volume | 51 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3NbtQwEB6hcoAL_9CUUhkJwSlt7Nhxc1wtLVsqcqio6M1yYkdatZugZFfq9sQj9Bn7JIydTegiKiS4Ockk8c_Y_mzPfAPwjpeikDHloY1MFPI0p6GWRoSyjITmUiCCdc7JX7Jkcso_n4mzW178HT_EsOHmeoYfr10H13m794s01HlgewpOnNSk8zJ3BlsOFZ0M_FEMlbNzL4rj0EWh71kbI7a3_vrarHTfVfDlnyDnOoL1U9DhY9B95jvLk_PdxTzfLa5-43X8n9I9gUcrfEpGnUI9hXu2egYPxn1YuOcw9d6b9cwiar-YFsSbyFfTxYzoypCjZmpc2k-BpW1uflxPlqapUU29CpCx2y5atvOWeGMFMq5tdbWcWZKNPk6IbonGW10QoBdwenjwdTwJV_EawgJhB7avyGMjChwyIksLyw0TeRqZxC9EGJfSakxbExkbR3ofx1qJ-CTVuObLk5Tz-CVsVHVlN4FwWpaa7udcaPxOYbUoWSo1gk2T05KmAYR9e6liRWbuYmpcqI6GmSlXgWqowAA-DPLfOxqPOyXf--YfxHRz7ozfpFDfsk_qODtmGUJAdRLAdq8fatXvW4X4KUlcWC8WwNvhMbaQO4bRla0XKCPxX4hcY5Qhd8ggakwpQ-gbwKtO9Yb8eMyFq-YAmFegv5RHjbKjg-Fq619eeg0PMc3cGRpNtmFj3izsG4Ri83zHd7efpdMo-w |
| linkProvider | Wiley-Blackwell |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1Lb9QwEB5BeyiXljeBAkZCcEqbOHbcHFfblizb5lC1gpvlxI60ajepsrsS21N_Ar-RX8LY2QQtokKCWx7jxI-x_dme-QbgPSt5IaKQ-SbQgc-SPPSV0NwXZcAVExwRrHVOPs3i9IJ9_so7a0LrC9PyQ_QbbrZnuPHadnC7Ib3_izXUumA7Dk6c1QS_D5s2rLcNYnB41jNIUVTP1sEoinwbh77jbQzo_nr6tXlp01bxtz-BznUM6yah4x3Iu-y3tieXe4t5vlfc_Mbs-F_lewjbK4hKBq1OPYJ7pnoMW8MuMtwTmDgHznpqELhfTQrirOSryWJKVKXJqJloe-1mwdI0P26_p0vd1KipTgvI0O4YLWfzGXH2CmRYm-pmOTUkGxymRM2IwkdtHKCncHF8dD5M_VXIBr9A5IFNzPNI8wJHjcCEhWGa8jwJdOzWIpQJYRReGx1oEwXqAIdbgRAlUbjsy-OEsegZbFR1ZV4AYWFZqvAgZ1zhdwqjeEkToRBv6jwsw8QDv2swWaz4zG1YjSvZMjFTaStQ9hXowcde_rpl8rhT8oNr_15MNZfW_k1w-SX7JMfZmGaIAuWZB7udgshV159JhFBxbCN7UQ_e9a-xhexJjKpMvUAZgf9C8BqhDLlDBoFjElJEvx48b3Wvz4-DXbhw9oA6DfpLeeQgGx31dy__JdFb2ErPT0_kySgbv4IH-JzaI7Uw3oWNebMwrxGZzfM3ru_9BCY0LRU |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3dbtMwFD4amwTcsPEzCBtgJARX2RLHjpfLqltpKURoYmJ3lhM7UrU1mdJWorviEXhGnoRjpwkUMSHBneOcJI59jv3553wH4BUreC6ikPkm0IHPkiz0ldDcF0XAFRMcEax1Tv6QxsMz9u6cn__ixd_wQ3QLbtYyXH9tDfxKF4c_SUOtB7aj4MRBTfBbsMVitBgLi047AimK2tn4F0WRb8PQt7SNAT1cf35tWNqyNfzlT5hzHcK6MWiwDaotfXP05OJgMc8O8uvfiB3_5_d24N4KoJJeo1H3YcOUD-BOv40L9xAmzn2zmhqE7ZeTnLgz8uVkMSWq1GRUT7RNuzGwMPX3r9-GS11XqKdOB0jfrhctZ_MZcacVSL8y5fVyakjaOx4SNSMKs5ooQI_gbHDyqT_0VwEb_BxxBzYwzyLNc-wzAhPmhmnKsyTQsZuJUCaEUZg2OtAmCtQRdrYCAUqicNKXxQlj0S5sllVpngBhYVGo8ChjXOF7cqN4QROhEG3qLCzCxAO_bS-Zr9jMbVCNS9nwMFNpK1B2FejBm07-quHxuFHytWv-TkzVF_b0m-Dyc_pWjtMxTREDylMP9lv9kCvDn0kEUHFs43pRD152t7GF7D6MKk21QBmB30LoGqEMuUEGYWMSUsS-HjxuVK8rjwNdOG32gDoF-sv_yF46Oumunv7LQy_g9sfjgXw_Ssd7cBezqd1PC-N92JzXC_MMYdk8e-4s7weP7yvN |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Organometallic+ruthenium+and+iridium+transfer-hydrogenation+catalysts+using+coenzyme+NADH+as+a+cofactor&rft.jtitle=Angewandte+Chemie+International+Edition&rft.au=Betanzos-Lara%2C+Soledad&rft.au=Liu%2C+Zhe&rft.au=Habtemariam%2C+Abraha&rft.au=Pizarro%2C+Ana+M&rft.date=2012-04-16&rft.eissn=1521-3773&rft.volume=51&rft.issue=16&rft.spage=3897&rft_id=info:doi/10.1002%2Fanie.201108175&rft_id=info%3Apmid%2F22415924&rft.externalDocID=22415924 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1433-7851&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1433-7851&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1433-7851&client=summon |