An Enantioselective Two-Component Catalyst System: Rh−Pd-Catalyzed Allylic Alkylation of Activated Nitriles
Saved in:
Published in | Journal of the American Chemical Society Vol. 118; no. 13; pp. 3309 - 3310 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
WASHINGTON
American Chemical Society
03.04.1996
Amer Chemical Soc |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Author | Ito, Yoshihiko Sudoh, Masaki Sawamura, Masaya |
---|---|
Author_xml | – sequence: 1 givenname: Masaya surname: Sawamura fullname: Sawamura, Masaya – sequence: 2 givenname: Masaki surname: Sudoh fullname: Sudoh, Masaki – sequence: 3 givenname: Yoshihiko surname: Ito fullname: Ito, Yoshihiko |
BookMark | eNqNkM9O20AQxldVkBqgh76BLz1UyLD_bK97s5xAK0WQlnBebTZjdRNnN_JugHDiSK99RJ6EBVc59cBlRqP5zaf5vkM0sM4CQp8JPiWYkrOlKjNOKYMPaEgyitOM0HyAhhhjmhYiZx_RoffLOHIqyBBtKpuMrbLBOA8t6GBuIZndubR2602UtiGpVVDtzofkOhZYf3t-_JP8-v389He6SPvdAyySqm13rdGxr3atinI2cU1SvQqqEPeXJnSmBX-MDhrVevj0rx-hm_PxrP6eTq4uftTVJFUsJyG-mgmRUVhgaCjwUlNCQYtioQmjJTDNG8pLXioBwBSm0TQ0OJ_zOSOFwIwdoa-9ru6c9x00ctOZtep2kmD5GpXcRxVZ0bN3MHeN1washj1fkbLMb0Y85zE1JmoT3uzVbmtDPD15_2mk0542Mcn7Paa6lcwLVmRyNr2Wl6MJnmbnP2UZ-S89r7SXS7ftbIzsPwZeAG4YnIY |
CitedBy_id | crossref_primary_10_1002_cjoc_202100824 crossref_primary_10_1002_anie_201208612 crossref_primary_10_1021_acs_orglett_0c03588 crossref_primary_10_1055_a_1696_5713 crossref_primary_10_1016_j_tetlet_2004_07_002 crossref_primary_10_1021_ma8020745 crossref_primary_10_1021_jacs_8b11868 crossref_primary_10_1002_adsc_200505149 crossref_primary_10_1002_ange_202203448 crossref_primary_10_1021_om970532x crossref_primary_10_1016_S0010_8545_98_00149_0 crossref_primary_10_1002_ange_200605113 crossref_primary_10_1021_acscatal_7b02909 crossref_primary_10_1055_s_0042_1751568 crossref_primary_10_1039_C5RA11432B crossref_primary_10_1248_cpb_56_1213 crossref_primary_10_1039_b925236n crossref_primary_10_1039_C6DT04513H crossref_primary_10_1021_ja0301469 crossref_primary_10_1002_ejic_200800308 crossref_primary_10_1002_chem_200701315 crossref_primary_10_1021_ol301272r crossref_primary_10_1021_ol402949t crossref_primary_10_1002_anie_202208837 crossref_primary_10_1016_j_tetlet_2009_09_005 crossref_primary_10_1021_ol005694v crossref_primary_10_1021_jacs_0c08348 crossref_primary_10_1039_C9SC05970A crossref_primary_10_1002_ange_202210086 crossref_primary_10_1039_C5OB00986C crossref_primary_10_1021_jo961343b crossref_primary_10_1039_D1CC05952A crossref_primary_10_1002_ejoc_202200499 crossref_primary_10_1039_c2sc00907b crossref_primary_10_1002_anie_201309698 crossref_primary_10_1016_0957_4166_96_00385_0 crossref_primary_10_1021_ja045532k crossref_primary_10_1016_j_jorganchem_2009_10_001 crossref_primary_10_1016_j_tetasy_2004_04_033 crossref_primary_10_1002_ejoc_201402911 crossref_primary_10_1002_anie_201407400 crossref_primary_10_1039_D3QO01605F crossref_primary_10_1021_acs_orglett_3c00323 crossref_primary_10_1002_ejoc_202201114 crossref_primary_10_1002_ange_200390301 crossref_primary_10_1002_anie_201912739 crossref_primary_10_1016_j_chempr_2018_03_010 crossref_primary_10_1002_anie_202111842 crossref_primary_10_1021_jacs_0c02316 crossref_primary_10_1021_om9705113 crossref_primary_10_1002_ange_202005019 crossref_primary_10_1002_anie_200802106 crossref_primary_10_1002_1521_3773_20020902_41_17_3230__AID_ANIE3230_3_0_CO_2_W crossref_primary_10_1021_acs_joc_6b00280 crossref_primary_10_1039_D0OB02499F crossref_primary_10_1021_ol7020669 crossref_primary_10_1002_ange_202208411 crossref_primary_10_1021_acs_orglett_6b00819 crossref_primary_10_1021_acs_chemrev_7b00385 crossref_primary_10_1016_j_tet_2013_05_106 crossref_primary_10_1002_asia_201601571 crossref_primary_10_1021_acscatal_1c01626 crossref_primary_10_1002_chem_201103892 crossref_primary_10_5059_yukigoseikyokaishi_75_1133 crossref_primary_10_1002_aoc_4166 crossref_primary_10_1016_S1872_2067_21_64051_2 crossref_primary_10_1002_ange_201208612 crossref_primary_10_1016_j_jorganchem_2008_09_049 crossref_primary_10_1246_bcsj_20110307 crossref_primary_10_1021_jacs_8b02783 crossref_primary_10_1038_s41467_021_23990_4 crossref_primary_10_1246_bcsj_70_2807 crossref_primary_10_1016_S0957_4166_99_00009_9 crossref_primary_10_1016_j_tet_2007_06_025 crossref_primary_10_1021_jacs_7b05460 crossref_primary_10_1039_C8QO00604K crossref_primary_10_1002_chem_201404015 crossref_primary_10_1002_ange_201407400 crossref_primary_10_1039_C5SC03597J crossref_primary_10_1295_koron_68_427 crossref_primary_10_1021_jacs_8b06458 crossref_primary_10_1002_adsc_201800986 crossref_primary_10_1021_acscatal_7b01833 crossref_primary_10_1021_ja303116v crossref_primary_10_1002_1521_3757_20020902_114_17_3364__AID_ANGE3364_3_0_CO_2_Z crossref_primary_10_1039_C9CC08559A crossref_primary_10_1002_ejic_200200671 crossref_primary_10_1021_ol034146p crossref_primary_10_1039_b905629g crossref_primary_10_1016_S0957_4166_98_00251_1 crossref_primary_10_5059_yukigoseikyokaishi_69_763 crossref_primary_10_1039_C9QO00667B crossref_primary_10_1021_om800448b crossref_primary_10_1038_ncomms6405 crossref_primary_10_1039_C7CC08732B crossref_primary_10_1021_om990710h crossref_primary_10_1021_jacs_9b05464 crossref_primary_10_1039_b802416b crossref_primary_10_1021_acscatal_2c04926 crossref_primary_10_1039_C5CY00133A crossref_primary_10_1246_bcsj_20170392 crossref_primary_10_1002_zaac_200800107 crossref_primary_10_1002_ange_201203066 crossref_primary_10_1002_adsc_201801148 crossref_primary_10_1002_anie_200390330 crossref_primary_10_1002_anie_200602482 crossref_primary_10_1021_ja204817y crossref_primary_10_1021_ja8077208 crossref_primary_10_1021_ja003774o crossref_primary_10_1021_om800667c crossref_primary_10_1016_j_tetasy_2005_02_009 crossref_primary_10_1016_S0040_4020_98_00319_6 crossref_primary_10_1021_jo026178g crossref_primary_10_1002_cjoc_202100002 crossref_primary_10_1002_anie_201203066 crossref_primary_10_1021_acs_orglett_9b02728 crossref_primary_10_1021_ja900257k crossref_primary_10_1021_cr000427o crossref_primary_10_1002_ange_19971092323 crossref_primary_10_1002_anie_201505805 crossref_primary_10_1021_acs_orglett_0c01687 crossref_primary_10_1021_jo302643v crossref_primary_10_1021_ol4009393 crossref_primary_10_1002_ange_200602482 crossref_primary_10_1021_om970464e crossref_primary_10_1002_anie_201504964 crossref_primary_10_1002_chem_200400666 crossref_primary_10_1002_ange_201309698 crossref_primary_10_1002_anie_202005019 crossref_primary_10_1016_j_tetlet_2005_07_139 crossref_primary_10_1007_s11426_022_1547_0 crossref_primary_10_1021_acs_chemrev_0c00564 crossref_primary_10_1016_j_checat_2022_10_031 crossref_primary_10_1016_S0040_4039_01_01467_8 crossref_primary_10_1021_acs_joc_3c00557 crossref_primary_10_1039_C7OB02476B crossref_primary_10_1002_ange_202111842 crossref_primary_10_1021_jacs_5b02810 crossref_primary_10_1002_ange_202305638 crossref_primary_10_1021_acs_orglett_7b02577 crossref_primary_10_1002_anie_199726351 crossref_primary_10_1016_j_tetasy_2006_09_011 crossref_primary_10_1002_ejic_200900435 crossref_primary_10_1039_c2cs35129c crossref_primary_10_1002_chem_201304284 crossref_primary_10_1002_ange_202208837 crossref_primary_10_1002_ejic_200400929 crossref_primary_10_1002_chem_200390202 crossref_primary_10_1016_j_tetlet_2005_01_082 crossref_primary_10_1016_j_jorganchem_2007_08_029 crossref_primary_10_1021_cr1003634 crossref_primary_10_1002_ange_200802106 crossref_primary_10_1002_anie_202208411 crossref_primary_10_1002_nadc_19970450209 crossref_primary_10_1016_j_jorganchem_2007_08_021 crossref_primary_10_1016_j_jcat_2022_11_025 crossref_primary_10_1039_C7QO00858A crossref_primary_10_1039_D1CY01804C crossref_primary_10_1002_adsc_201801346 crossref_primary_10_1002_chem_202304289 crossref_primary_10_1002_ange_200504021 crossref_primary_10_1016_S0010_8545_97_00067_2 crossref_primary_10_1021_ol0508328 crossref_primary_10_1021_ja961373w crossref_primary_10_1021_ja994387l crossref_primary_10_3762_bjoc_12_127 crossref_primary_10_1021_jo2004204 crossref_primary_10_1002_chem_202104268 crossref_primary_10_1038_s41467_023_44336_2 crossref_primary_10_1021_jacs_0c02150 crossref_primary_10_1016_j_molstruc_2008_04_007 crossref_primary_10_1002_chem_201900822 crossref_primary_10_1002_ejoc_201201761 crossref_primary_10_1002_anie_200504021 crossref_primary_10_1021_acs_orglett_6b02958 crossref_primary_10_1021_ol0067033 crossref_primary_10_1021_jacs_7b01931 crossref_primary_10_1002_ejoc_201501290 crossref_primary_10_1016_S0957_4166_00_00299_8 crossref_primary_10_1016_S0957_4166_99_00129_9 crossref_primary_10_1002_anie_202305638 crossref_primary_10_1002_ejoc_201200223 crossref_primary_10_1246_bcsj_73_2559 crossref_primary_10_1021_cr030700x crossref_primary_10_1002_chem_202100075 crossref_primary_10_1021_ol4006008 crossref_primary_10_1002_chem_201003383 crossref_primary_10_1021_ja029341y crossref_primary_10_1002_adsc_200900906 crossref_primary_10_1016_j_molstruc_2020_128124 crossref_primary_10_1021_acs_chemrev_0c00245 crossref_primary_10_1016_S0022_328X_97_00366_5 crossref_primary_10_1039_D0SC04959J crossref_primary_10_1002_ange_201912739 crossref_primary_10_1016_S0040_4039_97_01309_9 crossref_primary_10_1021_ic980433r crossref_primary_10_1002_ange_201503851 crossref_primary_10_1021_om300219f crossref_primary_10_1039_C6SC05556G crossref_primary_10_1016_S0957_4166_98_00391_7 crossref_primary_10_1016_j_tetlet_2007_07_020 crossref_primary_10_1021_acs_joc_8b00583 crossref_primary_10_1039_C9QO01089K crossref_primary_10_1021_ja971523i crossref_primary_10_1002_chin_199630050 crossref_primary_10_1021_cs501601c crossref_primary_10_1039_oc093197 crossref_primary_10_1002_anie_202210086 crossref_primary_10_1002_ange_201505805 crossref_primary_10_1360_TB_2023_0178 crossref_primary_10_1002_asia_200700183 crossref_primary_10_1039_C9PY00594C crossref_primary_10_1002_anie_202203448 crossref_primary_10_1002_anie_201503851 crossref_primary_10_1016_j_tet_2010_11_069 crossref_primary_10_1021_acscatal_6b01110 crossref_primary_10_1021_jacs_8b00187 crossref_primary_10_1002_ejic_200600771 crossref_primary_10_1021_jacs_0c08283 crossref_primary_10_1002_adsc_201400404 crossref_primary_10_1016_S0022_328X_00_00049_8 crossref_primary_10_1002_anie_200351170 crossref_primary_10_1002_anie_200605113 crossref_primary_10_1016_j_tet_2007_04_051 crossref_primary_10_1021_acs_orglett_8b02902 crossref_primary_10_1021_jacs_1c01880 crossref_primary_10_1021_om049112f crossref_primary_10_1016_S0040_4039_96_02329_5 crossref_primary_10_1021_acscatal_5b02692 crossref_primary_10_1016_j_tetlet_2007_03_065 crossref_primary_10_1021_jo502074s crossref_primary_10_1021_ja2029602 crossref_primary_10_1002_ange_200351170 crossref_primary_10_1002_ejoc_201600725 crossref_primary_10_1002_ange_201504964 crossref_primary_10_1021_ol801644f crossref_primary_10_1002_chem_200902818 crossref_primary_10_1021_ja5080135 crossref_primary_10_1016_S0040_4039_98_02603_3 |
Cites_doi | 10.1016/0040-4039(91)85092-J 10.1021/ja00534a029 10.1021/jo00355a025 10.1021/ja00033a035 10.1021/ja00155a008 10.1016/0040-4039(95)01295-S 10.1021/ja00047a053 10.1016/S0957-4166(00)86110-8 10.1021/jo00209a032 10.1021/om00010a020 10.1246/cl.1993.2057 10.1016/S0040-4020(01)89377-7 10.1021/ja00197a073 10.1246/cl.1991.2127 |
ContentType | Journal Article |
Copyright | Copyright © 1996 American Chemical Society |
Copyright_xml | – notice: Copyright © 1996 American Chemical Society |
DBID | BSCLL 1KM 1KN BLEPL DTL FCAKS AAYXX CITATION |
DOI | 10.1021/ja954223e |
DatabaseName | Istex Index Chemicus Current Chemical Reactions Web of Science Core Collection Science Citation Index Expanded Web of Science - Science Citation Index Expanded - 1996 CrossRef |
DatabaseTitle | Web of Science CrossRef |
Database_xml | – sequence: 1 dbid: 1KN name: Current Chemical Reactions url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.CCR sourceTypes: Enrichment Source Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 1520-5126 |
EndPage | 3310 |
ExternalDocumentID | 10_1021_ja954223e A1996UD46400038 ark_67375_TPS_NDL0P5FQ_9 c123084673 |
GroupedDBID | - .K2 02 186 3EH 3O- 41 53G 55A 5GY 5RE 5VS 7~N 85S AABXI AAYJJ ABDEX ABFLS ABMVS ABPPZ ABPTK ABUCX ABUFD ABWLT ACGFS ACJ ACNCT ACS ADKFC AEESW AENEX AETEA AFDAS AFEFF AFFDN AFFNX AFMIJ AIDAL ALMA_UNASSIGNED_HOLDINGS ANTXH AQSVZ BAANH CS3 D0S DU5 DZ EBS ED ED~ EJD ET F20 F5P GJ GNL IH9 IHE JG JG~ K2 K78 LG6 MVM NHB OHT P-O P2P ROL RXW TAE TAF TN5 UHB UI2 UKR UNC UPT UQL VF5 VG9 VH1 VQA W1F WH7 X XFK YXE YZZ ZCG ZGI ZHY ZY4 --- -DZ -ET -~X .DC .GJ 41~ 6TJ AAHBH AAYOK ABJNI ABQRX ABTAH ACBEA ACGFO ADHLV ADOJD AGXLV AHGAQ AI. BSCLL CUPRZ GGK IH2 XOL XSW YQT YYP ZCA ~02 1KM 1KN BLEPL DTL GROUPED_WOS_SCIENCE_CITATION_INDEX_EXPANDED AAYXX CITATION |
ID | FETCH-LOGICAL-a361t-7858852ed0ef2e49c212ec87dc1329e3c4f24949a8ee3a02542ef06b4b3178033 |
IEDL.DBID | ACS |
ISICitedReferencesCount | 270 |
ISICitedReferencesURI | https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=A1996UD46400038 |
ISSN | 0002-7863 |
IngestDate | Thu Sep 26 17:47:00 EDT 2024 Wed Sep 18 05:46:21 EDT 2024 Fri Oct 25 20:23:53 EDT 2024 Wed Oct 30 09:39:33 EDT 2024 Thu Aug 27 13:44:38 EDT 2020 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 13 |
Keywords | ALDOL CARBOXYLATES STEREOCHEMISTRY REGIOCHEMISTRY COMPLEXES CHIRAL DIPHOSPHINE LIGAND MICHAEL REACTIONS |
Language | English |
LinkModel | DirectLink |
LogoURL | https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg |
MergedId | FETCHMERGED-LOGICAL-a361t-7858852ed0ef2e49c212ec87dc1329e3c4f24949a8ee3a02542ef06b4b3178033 |
Notes | istex:A59AB2FF80B43BC909B5A2C98B245027E56BD5AC ark:/67375/TPS-NDL0P5FQ-9 |
PageCount | 2 |
ParticipantIDs | webofscience_primary_A1996UD46400038CitationCount webofscience_primary_A1996UD46400038 acs_journals_10_1021_ja954223e crossref_primary_10_1021_ja954223e istex_primary_ark_67375_TPS_NDL0P5FQ_9 |
ProviderPackageCode | JG~ 55A AABXI GNL VF5 7~N ACJ VG9 W1F ANTXH ACS AEESW AFEFF .K2 ABMVS ABUCX IH9 BAANH AQSVZ ED~ UI2 |
PublicationCentury | 1900 |
PublicationDate | 1996-04-03 |
PublicationDateYYYYMMDD | 1996-04-03 |
PublicationDate_xml | – month: 04 year: 1996 text: 1996-04-03 day: 03 |
PublicationDecade | 1990 |
PublicationPlace | WASHINGTON |
PublicationPlace_xml | – name: WASHINGTON |
PublicationTitle | Journal of the American Chemical Society |
PublicationTitleAbbrev | J AM CHEM SOC |
PublicationTitleAlternate | J. Am. Chem. Soc |
PublicationYear | 1996 |
Publisher | American Chemical Society Amer Chemical Soc |
Publisher_xml | – name: American Chemical Society – name: Amer Chemical Soc |
References | PAGANELLI, S (WOS:A1991FN52400031) 1991; 32 SAWAMURA, M (WOS:A1991FY88100010) 1991; 2 SAWAMURA, M (WOS:A1992HK67100035) 1992; 114 HAYASHI, T (WOS:A1986A394700025) 1986; 51 TROST, BM (WOS:A1980JY64500029) 1980; 102 SAWAMURA, M (WOS:A1994NF66700015) 1994; 50 SAWAMURA, M (WOS:A1995RU19300033) 1995; 36 SAWAMURA, M (WOS:A1995RY97100020) 1995; 14 SAWAMURA, M (WOS:A1992JR86300053) 1992; 114 TUJI J (WOS:A1996UD46400038.15) 1985; 50 Murahashi, SI (WOS:A1995TL73300008) 1995; 117 MIZUHO, Y (WOS:A1991GW25500015) 1991 HIRANO, M (WOS:A1993MM32800019) 1993 NAOTA, T (WOS:A1989AG63700073) 1989; 111 SAWAMURA M (WOS:A1996UD46400038.13) Sawamura M. (ja954223eb00008/ja954223eb00008_3) 1992; 114 Trost B. M. (ja954223eb00008/ja954223eb00008_1) 1980; 102 Hayashi T. (ja954223eb00008/ja954223eb00008_2) 1986; 51 Sawamura M. (ja954223eb00003/ja954223eb00003_2) 1994; 50 Mizuho Y. (ja954223eb00005/ja954223eb00005_1) 1991 Sawamura M. (ja954223eb00002/ja954223eb00002_1) 1991; 2 Sawamura M. (ja954223eb00003/ja954223eb00003_1) 1992; 114 Hirano M. (ja954223eb00005/ja954223eb00005_2) 1993 Naota T. (ja954223eb00001/ja954223eb00001_1) 1989; 111 Murahashi S. (ja954223eb00001/ja954223eb00001_2) 1995; 117 Tuji J. (ja954223eb00006/ja954223eb00006_1) 1985; 50 Reaction (ja954223eb00004/ja954223eb00004_1) Paganelli S. (ja954223eb00001/ja954223eb00001_3) 1991; 32 Sawamura M. (ja954223eb00003/ja954223eb00003_3) 1995; 36 Sawamura M. (ja954223eb00002/ja954223eb00002_2) 1995; 14 |
References_xml | – volume: 117 start-page: 12436 year: 1995 ident: WOS:A1995TL73300008 article-title: Ruthenium-catalyzed aldol and Michael reactions of nitriles. Carbon-carbon bond formation by alpha-C-H activation of nitriles publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: Murahashi, SI – volume: 32 start-page: 2807 year: 1991 ident: WOS:A1991FN52400031 article-title: RHODIUM-CATALYZED MICHAEL ADDITIONS OF ACTIVATED NITRILES TO ALPHA,BETA-UNSATURATED ESTERS publication-title: TETRAHEDRON LETTERS contributor: fullname: PAGANELLI, S – volume: 50 start-page: 1523 year: 1985 ident: WOS:A1996UD46400038.15 publication-title: J ORG CHEM contributor: fullname: TUJI J – ident: WOS:A1996UD46400038.13 publication-title: UNPUB contributor: fullname: SAWAMURA M – volume: 2 start-page: 593 year: 1991 ident: WOS:A1991FY88100010 article-title: A TRANS-CHELATING CHIRAL DIPHOSPHINE LIGAND - SYNTHESIS OF 2,2''-BIS[1-(DIPHENYLPHOSPHINO)ETHYL]-1,1''-BIFERROCENE AND ITS COMPLEXES WITH PLATINUM(II) AND PALLADIUM(II) publication-title: TETRAHEDRON-ASYMMETRY contributor: fullname: SAWAMURA, M – volume: 111 start-page: 5954 year: 1989 ident: WOS:A1989AG63700073 article-title: RUTHENIUM-CATALYZED ALDOL AND MICHAEL REACTIONS OF ACTIVATED NITRILES publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: NAOTA, T – volume: 50 start-page: 4439 year: 1994 ident: WOS:A1994NF66700015 article-title: ASYMMETRIC MICHAEL REACTION OF ALPHA-CYANO CARBOXYLATES CATALYZED BY A RHODIUM COMPLEX WITH TRANS-CHELATING CHIRAL DIPHOSPHINE PHTRAP publication-title: TETRAHEDRON contributor: fullname: SAWAMURA, M – volume: 36 start-page: 6479 year: 1995 ident: WOS:A1995RU19300033 article-title: ASYMMETRIC MICHAEL REACTION OF AN ALPHA-CYANO WEINREB AMIDE CATALYZED BY A RHODIUM COMPLEX WITH TRANS-CHELATING CHIRAL DIPHOSPHINE PHTRAP publication-title: TETRAHEDRON LETTERS contributor: fullname: SAWAMURA, M – start-page: 2057 year: 1993 ident: WOS:A1993MM32800019 article-title: SYNTHESIS OF NOVEL RHENIUM(I) ENOLATE COMPLEXES AS ACTIVE KEY INTERMEDIATES IN THE CATALYTIC ALDOL-TYPE REACTION publication-title: CHEMISTRY LETTERS contributor: fullname: HIRANO, M – volume: 51 start-page: 723 year: 1986 ident: WOS:A1986A394700025 article-title: STEREOCHEMISTRY AND REGIOCHEMISTRY IN PALLADIUM-CATALYZED NUCLEOPHILIC-SUBSTITUTION OF OPTICALLY-ACTIVE (E)-ALLYL AND (Z)-ALLYL ACETATES publication-title: JOURNAL OF ORGANIC CHEMISTRY contributor: fullname: HAYASHI, T – volume: 14 start-page: 4549 year: 1995 ident: WOS:A1995RY97100020 article-title: SYNTHESIS AND STRUCTURES OF TRANS-CHELATING CHIRAL DIPHOSPHINE LIGANDS BEARING AROMATIC P-SUBSTITUENTS, (S,S)-(R,R)-2,2''-BIS[1-(DIARYLPHOSPHINO)ETHYL]-1,1''-BIFFERROCENES AND (R,R)-(S,S)-2,2''-BIS[1-(DIARYLPHOSPHINO)ETHYL]-1,1''-BIFFERROCENES (ARYLTRAPS), AND THEIR TRANSITION-METAL COMPLEXES publication-title: ORGANOMETALLICS contributor: fullname: SAWAMURA, M – volume: 102 start-page: 4730 year: 1980 ident: WOS:A1980JY64500029 article-title: ALLYLIC ALKYLATION - PALLADIUM-CATALYZED SUBSTITUTIONS OF ALLYLIC CARBOXYLATES - STEREOCHEMISTRY AND REGIOCHEMISTRY publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: TROST, BM – volume: 114 start-page: 2586 year: 1992 ident: WOS:A1992HK67100035 article-title: CHIRAL PHOSPHINE-LIGANDS MODIFIED BY CROWN ETHERS - AN APPLICATION TO PALLADIUM-CATALYZED ASYMMETRIC ALLYLATION OF BETA-DIKETONES publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: SAWAMURA, M – start-page: 2127 year: 1991 ident: WOS:A1991GW25500015 article-title: C-H BOND ACTIVATION BY RUTHENIUM(0) COMPLEXES - ISOLATION OF AN ACTIVE INTERMEDIATE IN THE RUTHENIUM CATALYZED ALDOL AND MICHAEL REACTIONS publication-title: CHEMISTRY LETTERS contributor: fullname: MIZUHO, Y – volume: 114 start-page: 8295 year: 1992 ident: WOS:A1992JR86300053 article-title: CATALYTIC ASYMMETRIC-SYNTHESIS WITH TRANSCHELATING CHIRAL DIPHOSPHINE LIGAND TRAP - RHODIUM-CATALYZED ASYMMETRIC MICHAEL ADDITION OF ALPHA-CYANO CARBOXYLATES publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY contributor: fullname: SAWAMURA, M – volume: 32 start-page: 2807 year: 1991 ident: ja954223eb00001/ja954223eb00001_3 publication-title: Tetrahedron Lett. doi: 10.1016/0040-4039(91)85092-J contributor: fullname: Paganelli S. – volume: 102 start-page: 4730 year: 1980 ident: ja954223eb00008/ja954223eb00008_1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00534a029 contributor: fullname: Trost B. M. – volume: 51 start-page: 723 year: 1986 ident: ja954223eb00008/ja954223eb00008_2 publication-title: J. Org. Chem. doi: 10.1021/jo00355a025 contributor: fullname: Hayashi T. – volume: 114 start-page: 2586 year: 1992 ident: ja954223eb00008/ja954223eb00008_3 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00033a035 contributor: fullname: Sawamura M. – volume: 117 start-page: 12436 year: 1995 ident: ja954223eb00001/ja954223eb00001_2 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00155a008 contributor: fullname: Murahashi S. – volume: 36 start-page: 6479 year: 1995 ident: ja954223eb00003/ja954223eb00003_3 publication-title: Tetrahedron Lett. doi: 10.1016/0040-4039(95)01295-S contributor: fullname: Sawamura M. – volume: 114 start-page: 8295 year: 1992 ident: ja954223eb00003/ja954223eb00003_1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00047a053 contributor: fullname: Sawamura M. – volume: 2 start-page: 593 year: 1991 ident: ja954223eb00002/ja954223eb00002_1 publication-title: Tetrahedron: Asymmetry doi: 10.1016/S0957-4166(00)86110-8 contributor: fullname: Sawamura M. – volume: 50 start-page: 1523 year: 1985 ident: ja954223eb00006/ja954223eb00006_1 publication-title: J. Org. Chem. doi: 10.1021/jo00209a032 contributor: fullname: Tuji J. – volume: 14 start-page: 4549 year: 1995 ident: ja954223eb00002/ja954223eb00002_2 publication-title: Organometallics doi: 10.1021/om00010a020 contributor: fullname: Sawamura M. – start-page: 2057 year: 1993 ident: ja954223eb00005/ja954223eb00005_2 publication-title: Chem. Lett. doi: 10.1246/cl.1993.2057 contributor: fullname: Hirano M. – volume: 50 start-page: 4439 year: 1994 ident: ja954223eb00003/ja954223eb00003_2 publication-title: Tetrahedron doi: 10.1016/S0040-4020(01)89377-7 contributor: fullname: Sawamura M. – volume: 111 start-page: 5954 year: 1989 ident: ja954223eb00001/ja954223eb00001_1 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00197a073 contributor: fullname: Naota T. – start-page: 2127 year: 1991 ident: ja954223eb00005/ja954223eb00005_1 publication-title: Chem. Lett. doi: 10.1246/cl.1991.2127 contributor: fullname: Mizuho Y. – volume-title: M. ident: ja954223eb00004/ja954223eb00004_1 contributor: fullname: Reaction |
SSID | ssj0004281 |
Score | 2.0518537 |
Source | Web of Science |
SourceID | crossref webofscience istex acs |
SourceType | Aggregation Database Enrichment Source Index Database Publisher |
StartPage | 3309 |
SubjectTerms | Chemistry Chemistry, Multidisciplinary Physical Sciences Science & Technology |
Title | An Enantioselective Two-Component Catalyst System: Rh−Pd-Catalyzed Allylic Alkylation of Activated Nitriles |
URI | http://dx.doi.org/10.1021/ja954223e https://api.istex.fr/ark:/67375/TPS-NDL0P5FQ-9/fulltext.pdf http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=A1996UD46400038 |
Volume | 118 |
WOS | A1996UD46400038 |
WOSCitedRecordID | wosA1996UD46400038 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3JTsMwEB2xHODCjiibLEDcglLb2bhFKRVCUBVoJW6R4zqiatVWTRCUE0e48ol8CeOkYRHrKQdPImfGnjeJZ94A7MUskrGUOm3Q5AaPcad7VLiGhd5Sxo5E0NaFwmc1-7jJT66sqwnY_eEEn2p-IM_iCGJqEqapY3q6P4MfXL4XP1K3XMS4jmuzgj7o460aemTyCXqmtRbvvoWbDFqq81ApCnTyjJLOwU0aHcj7r3yNv816AebGoSXx87WwCBOqtwQzQdHRbRkGfo8c6cSXdj_J2t-gpyON276hnUK_h_BDAv03Z5SkJGcyP3x5eCIX1y-Pz_WWkY_dqxbxu91Rty3x2hnluXSkHxNfZq3ScLzWTofobZIVaFaPGsGxMe64YAhml1PUn-W6FlUtU8VUcU8isCnpOi2p-9ErJnlMNZ2NcJViQhfSUxWbdsQjDENck7FVmOrhfNeAKK4w1sLnMIy4IpsKR1hCeArDF05lmZZgG00SjndMEmaH4RQ_RgrFlWCnsFY4yJk3vhPaz-z4JiGGHZ2q5lhho34Z1iqnZt2qnodeCfY-GvpNXrP-2s0Kx6nqQ9ISlP8jFoz50zVvQLr-15tswGye680Nk23CVDq8UVsYyqTRdraUXwH0Oe21 |
link.rule.ids | 315,783,787,2774,27090,27938,27939,57072,57122 |
linkProvider | American Chemical Society |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9NAEB5BeygX3ojwKCtUcXPl7MMPbpbbKEAaBZpIvVnrzVpEiZIqdgXpiSNc-Yn9Jcys7bagSvTkw46t8ezufGPvzDcAe4XITWEMpQ360pMF7vSY68hT6C1NERoEbSoUPhoG_Yn8eKJOGpocqoVBJUp8UukO8a_YBYgmKFYSsczehW0V-iF1K0jS46saSB5121A3jALRsghdv5UQyJR_IdA2GfP7jajjEKb3oG5V5HRziSXz_bMq3zfn_9A23k75h3C_CTRZUq-MR3DHLh_DTtr2d3sCp8mSHVIazGxVumY46PfY-NvKIxexWiIYsZT-7WzKitW85u8vfvxiX75e_Pw9mnr12LmdsmSx2CxmBq_zTZ1Zx1YFS4xrnIbjw1m1Rt9TPoVJ73Cc9r2m_4KnRdCt0IwqihS3U98W3MrYIMxZE4VTQ93prTCy4ERuoyNrhaayem4LP8hljkFJ5AvxDLaWqO9zYFZajLzwOQLjrzzgOtRK69hiMCO56fIO7KLdsmb_lJk7Guf4adIargNv20nLTmsejpuE3rnpvJTQ6zklroUqG4-Os-HBwB-p3ucs7sDe9fm-lCcO4GByIFFVOjLtQPc2YmnDpk4sAtWL_73JG9jpj48G2eDD8NNLuFdngUvPF69gq1qf2dcY5FT5rlvdfwALNvYe |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9NAEF5BKwGX8qwIhbJCFTdX9j784GY5jQqUEGgi9Wat17siSpREsauSnnpsr_zE_hJm_AgFVaInH3a9Gs_uzjfrnfmGkD3LM221xrBBVzjCwk6PmAodCdZS20ADaGOi8Je-fzgSn07kSXNQxFwYEKKAkYrqEh939SK3DcMAUgVFUgCemftkUwYew4oFcXL8Jw-ShV7r7gahz1smoZuvIgrp4i8U2kSF_rwVeSqU6T0mX9fyVcElk_3TMtvX5_9QN979A56QrcbhpHG9Qp6Se2b2jDxM2jpvz8kintEDDIcZz4uqKA7YPzo8mztoKuYzACWa4D-eVVHSmt_8w_XFFf3-4_ry1yB36rZzk9N4Ol1Nxxqek1UdYUfnlsa6KqAG7f1xuQQbVLwgo97BMDl0mjoMjuK-V4IqZRhKZnLXWGZEpAHujA6DXGOVesO1sAxJblRoDFeYXs-Mdf1MZOCchC7n22RjBvK-JNQIAx4YjMPBD8t8pgIllYoMODWCaY91yC7oLm32UZFWV-QMjiit4jrkXTtx6aLm47it0_tqStc91HKCAWyBTIeD47TfPXIHsvctjTpk7-acr_sjF7A_6goQFa9OO8S7S7ekYVVHNoHy1f--5C15MOj20qOP_c875FEdDC4cl78mG-Xy1LwBX6fMdqsF_hv4X_iY |
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=An+Enantioselective+Two-Component+Catalyst+System%3A%E2%80%89+Rh%E2%88%92Pd-Catalyzed+Allylic+Alkylation+of+Activated+Nitriles&rft.jtitle=Journal+of+the+American+Chemical+Society&rft.au=SAWAMURA%2C+Masaya&rft.au=SUDOH%2C+Masaki&rft.au=ITO%2C+Yoshihiko&rft.date=1996-04-03&rft.pub=American+Chemical+Society&rft.issn=0002-7863&rft.eissn=1520-5126&rft.volume=118&rft.issue=13&rft.spage=3309&rft.epage=3310&rft_id=info:doi/10.1021%2Fja954223e&rft.externalDBID=n%2Fa&rft.externalDocID=ark_67375_TPS_NDL0P5FQ_9 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0002-7863&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0002-7863&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0002-7863&client=summon |