Pd(II)-Catalyzed Phosphorylation of Aryl C–H Bonds
A Pd(II)-catalyzed C–H phosphorylation reaction has been developed using heterocycle-directed ortho-palladation. Both H-phosphonates and diaryl phosphine oxides are suitable coupling partners for this reaction.
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Published in | Journal of the American Chemical Society Vol. 135; no. 25; pp. 9322 - 9325 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
WASHINGTON
American Chemical Society
26.06.2013
Amer Chemical Soc |
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Abstract | A Pd(II)-catalyzed C–H phosphorylation reaction has been developed using heterocycle-directed ortho-palladation. Both H-phosphonates and diaryl phosphine oxides are suitable coupling partners for this reaction. |
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AbstractList | A Pd(II)-catalyzed C-H phosphorylation reaction has been developed using heterocycle-directed ortho-palladation. Both H-phosphonates and diaryl phosphine oxides are suitable coupling partners for this reaction.A Pd(II)-catalyzed C-H phosphorylation reaction has been developed using heterocycle-directed ortho-palladation. Both H-phosphonates and diaryl phosphine oxides are suitable coupling partners for this reaction. A Pd(II)-catalyzed C–H phosphorylation reaction has been developed using heterocycle-directed ortho-palladation. Both H-phosphonates and diaryl phosphine oxides are suitable coupling partners for this reaction. |
Author | Li, Suhua Xiao, Kai-Jiong Ye, Mengchun Feng, Chen-Guo Yu, Jin-Quan |
AuthorAffiliation | The Scripps Research Institute |
AuthorAffiliation_xml | – name: The Scripps Research Institute |
Author_xml | – sequence: 1 givenname: Chen-Guo surname: Feng fullname: Feng, Chen-Guo – sequence: 2 givenname: Mengchun surname: Ye fullname: Ye, Mengchun – sequence: 3 givenname: Kai-Jiong surname: Xiao fullname: Xiao, Kai-Jiong – sequence: 4 givenname: Suhua surname: Li fullname: Li, Suhua – sequence: 5 givenname: Jin-Quan surname: Yu fullname: Yu, Jin-Quan email: yu200@scripps.edu |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23755825$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1021/ja806955s 10.2174/1385272033372761 10.1021/cr100280d 10.1021/jm101035x 10.1002/chem.200901473 10.1021/ol016971g 10.1021/om800906m 10.1021/cr020049i 10.1055/s-1981-29335 10.1016/j.tet.2013.04.067 10.1021/jm300037x 10.1246/cl.2007.200 10.1021/ja0570943 10.1021/ol052406s 10.1021/ol200465z 10.1021/om800641n 10.1016/S0022-328X(00)90525-4 10.1039/c2ob26874d 10.1021/ol201222n 10.1039/c3cc41107a 10.1021/ol062082n 10.1021/jo0343376 10.1021/ar9000058 10.1021/om9005615 10.1021/ol0346640 10.1021/ja0058738 10.1038/366529a0 10.1021/ja103834b 10.1021/ar200185g 10.1021/jo201030j 10.1039/a807830k 10.1002/adsc.200900590 10.1039/c2cc30429e 10.1021/jo025732j 10.1021/jo301108g 10.1021/ol051216e 10.1021/ja990702s 10.1016/S0022-328X(02)01857-0 10.1021/ja0646747 10.1021/ja00124a025 10.1021/jm0103211 10.1016/j.tet.2003.09.066 10.1021/ol016257z 10.1351/pac200779122217 10.1002/anie.200800497 10.1016/j.catcom.2008.02.017 10.1021/cr900184e 10.1021/cr2002646 10.1021/ol400732q 10.1021/ja3069165 10.1021/ma0116295 10.1021/cr2004212 10.1002/chem.201103723 10.1021/op034007n 10.1021/ja103776u 10.1021/ja042806v 10.1021/ar9900865 10.1016/j.tet.2012.05.040 10.1021/ja003361n 10.1039/b606984n 10.1039/c2ob25225b 10.1021/ol070406h 10.1055/s-0031-1289700 10.1002/1521-3773(20001002)39:19<3440::AID-ANIE3440>3.0.CO;2-1 10.1021/ol300582y 10.1055/s-0030-1257960 10.1021/ja301764m |
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References | Ueura K. (ref10/cit10a) 2007; 9 Lim C. W. (ref3/cit3d) 2003; 7 Trost B. M. (ref12/cit12b) 1995; 117 Xiang C.-B. (ref15/cit15c) 2012; 77 Chen X. (ref18/cit18a) 2006; 128 Jun C.-H. (ref12/cit12d) 2000; 39 Gelman D. (ref7/cit7a) 2003; 5 Stepanova V. A. (ref17/cit17c) 2009; 28 Helmchen G. (ref3/cit3a) 2000; 33 Stuart D. R. (ref10/cit10b) 2008; 130 Kraszewski A. (ref19/cit19) 2007; 79 Netherton M. R. (ref3/cit3b) 2001; 3 Ackermann L. (ref11/cit11c) 2005; 7 Oi S. (ref11/cit11b) 2001; 3 Guo Y. (ref3/cit3h) 2008; 9 Wang H. (ref15/cit15d) 2012; 44 Li Y. (ref3/cit3i) 2012; 134 Patureau F. W. (ref10/cit10c) 2010; 132 Zhuang R. (ref7/cit7c) 2011; 13 Andaloussi M. (ref6/cit6b) 2009; 15 Allcock H. R. (ref2/cit2a) 2002; 35 Chan L. Y. (ref13/cit13c) 2013; 49 Bolm C. (ref17/cit17b) 2002; 662 Tang W. (ref3/cit3e) 2003; 103 Onouchi H. (ref2/cit2b) 2005; 127 Seregin I. V. (ref9/cit9b) 2007; 36 Engle K. M. (ref9/cit9g) 2012; 45 Kataoka N. (ref3/cit3c) 2002; 67 Yu D.-G. (ref9/cit9f) 2012; 68 Murai S. (ref12/cit12a) 1993; 366 Surry D. S. (ref3/cit3g) 2008; 47 Weissman H. (ref11/cit11a) 2000; 123 Deal E. L. (ref6/cit6c) 2011; 13 Daugulis O. (ref9/cit9c) 2009; 42 Kalek M. (ref20/cit20b) 2008; 27 Shen C. (ref8/cit8d) 2012; 10 Chan L. Y. (ref13/cit13a) 2013; 15 ref8/cit8a Jeon W. H. (ref13/cit13b) 2013; 69 Lenges C. P. (ref12/cit12c) 1999; 121 Kalek M. (ref6/cit6a) 2009; 351 Chen X. (ref18/cit18b) 2006; 128 Kohler M. C. (ref20/cit20c) 2009; 28 Dang Q. (ref1/cit1b) 2011; 54 Van Allen D. (ref7/cit7b) 2003; 68 Hou C. (ref16/cit16) 2012; 48 Sokolov V. I. (ref17/cit17a) 1980; 202 Baillie C. (ref5/cit5a) 2003; 7 Kagayama T. (ref15/cit15a) 2006; 8 Tan K. L. (ref12/cit12e) 2001; 123 Chen X. (ref1/cit1c) 2012; 55 Queffélec C. (ref2/cit2c) 2012; 112 Demmer C. S. (ref5/cit5c) 2011; 111 Sawa M. (ref1/cit1a) 2002; 45 Tappe F. M. J. (ref5/cit5b) 2010 Lyons T. W. (ref9/cit9d) 2010; 110 Gaumont A.-C. (ref20/cit20a) 1999 Hirao T. (ref4/cit4) 1981 Rummelt S. M. (ref6/cit6d) 2012; 14 Zhang H.-Y. (ref8/cit8c) 2012; 10 Yeung C. S. (ref9/cit9e) 2011; 111 Hyster T. K. (ref10/cit10d) 2010; 132 Chelucci G. (ref3/cit3f) 2003; 59 Zhao Y.-L. (ref8/cit8b) 2012; 18 Satoh T. (ref9/cit9a) 2007; 36 Kuninobu Y. (ref14/cit14) 2011; 76 Mu X.-J. (ref15/cit15b) 2006; 8 Rummelt, SM (WOS:000302990100061) 2012; 14 Surry, DS (WOS:000258584800004) 2008; 47 Daugulis, O (WOS:000269308800009) 2009; 42 (000321236600023.2) 2004 Yeung, CS (WOS:000288820600003) 2011; 111 Tappe, FMJ (WOS:000282106400001) 2010 Bolm, C (WOS:000179271800004) 2002; 662 Wang, HL (WOS:000301344200015) 2012; 44 Seregin, IV (WOS:000247341300014) 2007; 36 HIRAO, T (WOS:A1981KZ04900019) 1981 Oi, S (WOS:000170392300041) 2001; 3 Guo, Y (WOS:000256183700010) 2008; 9 Kalek, M (WOS:000260791400017) 2008; 27 Engle, KM (WOS:000305321100003) 2012; 45 Xiang, CB (WOS:000308390100059) 2012; 77 Zhang, HY (WOS:000311755100011) 2012; 10 Ackermann, L (WOS:000230213100081) 2005; 7 MURAI, S (WOS:A1993ML21800059) 1993; 366 Kraszewski, A. (000321236600023.26) 2007; 79 Helmchen, G (WOS:000087894400004) 2000; 33 Chan, LY (WOS:000318028500030) 2013; 49 Sawa, M (WOS:000173985300018) 2002; 45 Onouchi, H (WOS:000227479600050) 2005; 127 Chen, XQ (WOS:000303173600018) 2012; 55 Ueura, K (WOS:000245084300059) 2007; 9 Satoh, T (WOS:000245866200001) 2007; 36 Tan, KL (WOS:000167632900034) 2001; 123 Chen, X (WOS:000240795000023) 2006; 128 Andaloussi, M (WOS:000273697100021) 2009; 15 Allcock, HR (WOS:000175112100026) 2002; 35 Kalek, M (WOS:000273394500028) 2009; 351 Mu, XJ (WOS:000241729500029) 2006; 8 Patureau, FW (WOS:000280227700019) 2010; 132 Kuninobu, Y (WOS:000294702000009) 2011; 76 Netherton, MR (WOS:000172939500043) 2001; 3 Hyster, TK (WOS:000280456100055) 2010; 132 Zhao, YL (WOS:000306670200024) 2012; 18 Weissman, H (WOS:000166498600021) 2001; 123 Li, YH (WOS:000305107800032) 2012; 134 Kataoka, N (WOS:000177318300013) 2002; 67 Demmer, CS (WOS:000297946600012) 2011; 111 Lyons, TW (WOS:000274705900016) 2010; 110 Jeon, WH (WOS:000319647600013) 2013; 69 Kagayama, T (WOS:000235120700014) 2006; 8 Shen, CR (WOS:000302420700017) 2012; 10 TROST, BM (WOS:A1995QY88500025) 1995; 117 (000321236600023.1) 2004 Lim, CW (WOS:000183051400025) 2003; 7 Tang, WJ (WOS:000184821500013) 2003; 103 Chen, X (WOS:000234547700039) 2006; 128 Chelucci, G (WOS:000186617600001) 2003; 59 SOKOLOV, VI (WOS:A1980KU31400018) 1980; 202 Zhuang, RQ (WOS:000289187200056) 2011; 13 Stepanova, VA (WOS:000271662700019) 2009; 28 Yu, DG (WOS:000305381700002) 2012; 68 Van Allen, D (WOS:000183066100070) 2003; 68 Baillie, C (WOS:000181184000004) 2003; 7 Deal, EL (WOS:000291409800076) 2011; 13 Dang, Q (WOS:000285818000012) 2011; 54 Chan, LY (WOS:000318588900030) 2013; 15 Queffelec, C (WOS:000306298800004) 2012; 112 Jun, CH (WOS:000089732100015) 2000; 39 Stuart, DR (WOS:000263320200016) 2008; 130 Kohler, MC (WOS:000263420400035) 2009; 28 Lenges, CP (WOS:000081603000010) 1999; 121 Hou, CD (WOS:000303320000036) 2012; 48 Gelman, D (WOS:000183692600031) 2003; 5 Gaumont, AC (WOS:000078130200029) 1999 |
References_xml | – volume: 130 start-page: 16474 year: 2008 ident: ref10/cit10b publication-title: J. Am. Chem. Soc. doi: 10.1021/ja806955s – volume: 7 start-page: 477 year: 2003 ident: ref5/cit5a publication-title: Curr. Org. Chem doi: 10.2174/1385272033372761 – volume: 111 start-page: 1215 year: 2011 ident: ref9/cit9e publication-title: Chem. Rev. doi: 10.1021/cr100280d – volume: 54 start-page: 153 year: 2011 ident: ref1/cit1b publication-title: J. Med. Chem. doi: 10.1021/jm101035x – volume: 15 start-page: 13069 year: 2009 ident: ref6/cit6b publication-title: Chem.—Eur. J. doi: 10.1002/chem.200901473 – volume: 3 start-page: 4295 year: 2001 ident: ref3/cit3b publication-title: Org. Lett. doi: 10.1021/ol016971g – volume: 28 start-page: 1193 year: 2009 ident: ref20/cit20c publication-title: Organometallics doi: 10.1021/om800906m – volume: 103 start-page: 3029 year: 2003 ident: ref3/cit3e publication-title: Chem. Rev. doi: 10.1021/cr020049i – start-page: 56 year: 1981 ident: ref4/cit4 publication-title: Synthesis doi: 10.1055/s-1981-29335 – volume: 69 start-page: 5152 year: 2013 ident: ref13/cit13b publication-title: Tetrahedron doi: 10.1016/j.tet.2013.04.067 – volume: 55 start-page: 3837 year: 2012 ident: ref1/cit1c publication-title: J. Med. Chem. doi: 10.1021/jm300037x – volume: 36 start-page: 200 year: 2007 ident: ref9/cit9a publication-title: Chem. Lett. doi: 10.1246/cl.2007.200 – volume: 128 start-page: 78 year: 2006 ident: ref18/cit18a publication-title: J. Am. Chem. Soc. doi: 10.1021/ja0570943 – volume: 8 start-page: 407 year: 2006 ident: ref15/cit15a publication-title: Org. Lett. doi: 10.1021/ol052406s – volume: 13 start-page: 2110 year: 2011 ident: ref7/cit7c publication-title: Org. Lett. doi: 10.1021/ol200465z – volume: 27 start-page: 5876 year: 2008 ident: ref20/cit20b publication-title: Organometallics doi: 10.1021/om800641n – volume: 202 start-page: C58 year: 1980 ident: ref17/cit17a publication-title: J. Organomet. Chem. doi: 10.1016/S0022-328X(00)90525-4 – volume: 10 start-page: 9627 year: 2012 ident: ref8/cit8c publication-title: Org. Biomol. Chem. doi: 10.1039/c2ob26874d – volume: 13 start-page: 3270 year: 2011 ident: ref6/cit6c publication-title: Org. Lett. doi: 10.1021/ol201222n – volume: 49 start-page: 4682 year: 2013 ident: ref13/cit13c publication-title: Chem. Commun. doi: 10.1039/c3cc41107a – ident: ref8/cit8a – volume: 8 start-page: 5291 year: 2006 ident: ref15/cit15b publication-title: Org. Lett. doi: 10.1021/ol062082n – volume: 68 start-page: 4590 year: 2003 ident: ref7/cit7b publication-title: J. Org. Chem. doi: 10.1021/jo0343376 – volume: 42 start-page: 1074 year: 2009 ident: ref9/cit9c publication-title: Acc. Chem. Res. doi: 10.1021/ar9000058 – volume: 28 start-page: 6546 year: 2009 ident: ref17/cit17c publication-title: Organometallics doi: 10.1021/om9005615 – volume: 5 start-page: 2315 year: 2003 ident: ref7/cit7a publication-title: Org. Lett. doi: 10.1021/ol0346640 – volume: 123 start-page: 2685 year: 2001 ident: ref12/cit12e publication-title: J. Am. Chem. Soc. doi: 10.1021/ja0058738 – volume: 366 start-page: 529 year: 1993 ident: ref12/cit12a publication-title: Nature doi: 10.1038/366529a0 – volume: 132 start-page: 9982 year: 2010 ident: ref10/cit10c publication-title: J. Am. Chem. Soc. doi: 10.1021/ja103834b – volume: 45 start-page: 788 year: 2012 ident: ref9/cit9g publication-title: Acc. Chem. Res. doi: 10.1021/ar200185g – volume: 76 start-page: 7370 year: 2011 ident: ref14/cit14 publication-title: J. Org. Chem. doi: 10.1021/jo201030j – start-page: 63 year: 1999 ident: ref20/cit20a publication-title: Chem. Commun. doi: 10.1039/a807830k – volume: 351 start-page: 3207 year: 2009 ident: ref6/cit6a publication-title: Adv. Synth. Catal. doi: 10.1002/adsc.200900590 – volume: 48 start-page: 5181 year: 2012 ident: ref16/cit16 publication-title: Chem. Commun. doi: 10.1039/c2cc30429e – volume: 67 start-page: 5553 year: 2002 ident: ref3/cit3c publication-title: J. Org. Chem. doi: 10.1021/jo025732j – volume: 77 start-page: 7706 year: 2012 ident: ref15/cit15c publication-title: J. Org. Chem. doi: 10.1021/jo301108g – volume: 7 start-page: 3123 year: 2005 ident: ref11/cit11c publication-title: Org. Lett. doi: 10.1021/ol051216e – volume: 121 start-page: 6616 year: 1999 ident: ref12/cit12c publication-title: J. Am. Chem. Soc. doi: 10.1021/ja990702s – volume: 662 start-page: 23 year: 2002 ident: ref17/cit17b publication-title: J. Organomet. Chem. doi: 10.1016/S0022-328X(02)01857-0 – volume: 128 start-page: 12634 year: 2006 ident: ref18/cit18b publication-title: J. Am. Chem. Soc. doi: 10.1021/ja0646747 – volume: 117 start-page: 5371 year: 1995 ident: ref12/cit12b publication-title: J. Am. Chem. Soc. doi: 10.1021/ja00124a025 – volume: 45 start-page: 919 year: 2002 ident: ref1/cit1a publication-title: J. Med. Chem. doi: 10.1021/jm0103211 – start-page: 3037 year: 2010 ident: ref5/cit5b publication-title: Synthesis – volume: 59 start-page: 9471 year: 2003 ident: ref3/cit3f publication-title: Tetrahedron doi: 10.1016/j.tet.2003.09.066 – volume: 3 start-page: 2579 year: 2001 ident: ref11/cit11b publication-title: Org. Lett. doi: 10.1021/ol016257z – volume: 79 start-page: 2217 year: 2007 ident: ref19/cit19 publication-title: Pure Appl. Chem. doi: 10.1351/pac200779122217 – volume: 47 start-page: 6338 year: 2008 ident: ref3/cit3g publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.200800497 – volume: 9 start-page: 1842 year: 2008 ident: ref3/cit3h publication-title: Catal. Commun. doi: 10.1016/j.catcom.2008.02.017 – volume: 110 start-page: 1147 year: 2010 ident: ref9/cit9d publication-title: Chem. Rev. doi: 10.1021/cr900184e – volume: 111 start-page: 7981 year: 2011 ident: ref5/cit5c publication-title: Chem. Rev. doi: 10.1021/cr2002646 – volume: 15 start-page: 2186 year: 2013 ident: ref13/cit13a publication-title: Org. Lett. doi: 10.1021/ol400732q – volume: 134 start-page: 18325 year: 2012 ident: ref3/cit3i publication-title: J. Am. Chem. Soc. doi: 10.1021/ja3069165 – volume: 35 start-page: 3484 year: 2002 ident: ref2/cit2a publication-title: Macromolecules doi: 10.1021/ma0116295 – volume: 112 start-page: 3777 year: 2012 ident: ref2/cit2c publication-title: Chem. Rev. doi: 10.1021/cr2004212 – volume: 18 start-page: 9622 year: 2012 ident: ref8/cit8b publication-title: Chem.—Eur. J. doi: 10.1002/chem.201103723 – volume: 7 start-page: 379 year: 2003 ident: ref3/cit3d publication-title: Org Process Res Dev doi: 10.1021/op034007n – volume: 132 start-page: 10565 year: 2010 ident: ref10/cit10d publication-title: J. Am. Chem. Soc. doi: 10.1021/ja103776u – volume: 127 start-page: 2960 year: 2005 ident: ref2/cit2b publication-title: J. Am. Chem. Soc. doi: 10.1021/ja042806v – volume: 33 start-page: 336 year: 2000 ident: ref3/cit3a publication-title: Acc. Chem. Res. doi: 10.1021/ar9900865 – volume: 68 start-page: 5130 year: 2012 ident: ref9/cit9f publication-title: Tetrahedron doi: 10.1016/j.tet.2012.05.040 – volume: 123 start-page: 337 year: 2000 ident: ref11/cit11a publication-title: J. Am. Chem. Soc. doi: 10.1021/ja003361n – volume: 36 start-page: 1173 year: 2007 ident: ref9/cit9b publication-title: Chem. Soc. Rev. doi: 10.1039/b606984n – volume: 10 start-page: 3500 year: 2012 ident: ref8/cit8d publication-title: Org. Biomol. Chem. doi: 10.1039/c2ob25225b – volume: 9 start-page: 1407 year: 2007 ident: ref10/cit10a publication-title: Org. Lett. doi: 10.1021/ol070406h – volume: 44 start-page: 941 year: 2012 ident: ref15/cit15d publication-title: Synthesis doi: 10.1055/s-0031-1289700 – volume: 39 start-page: 3440 year: 2000 ident: ref12/cit12d publication-title: Angew. Chem., Int. Ed. doi: 10.1002/1521-3773(20001002)39:19<3440::AID-ANIE3440>3.0.CO;2-1 – volume: 14 start-page: 2188 year: 2012 ident: ref6/cit6d publication-title: Org. Lett. doi: 10.1021/ol300582y – volume: 9 start-page: 1842 year: 2008 ident: WOS:000256183700010 article-title: Synthesis of new triarylphosphine ligand and their application in styrene hydroformylation publication-title: CATALYSIS COMMUNICATIONS doi: 10.1016/j.catcom.2008.02.017 – volume: 7 start-page: 3123 year: 2005 ident: WOS:000230213100081 article-title: Phosphine oxides as preligands in ruthenium-catalyzed arylations via C-H bond functionalization using aryl chlorides publication-title: ORGANIC LETTERS doi: 10.1021/ol051216e – volume: 18 start-page: 9622 year: 2012 ident: WOS:000306670200024 article-title: [NiCl2(dppp)]-Catalyzed Cross-Coupling of Aryl Halides with Dialkyl Phosphite, Diphenylphosphine Oxide, and Diphenylphosphine publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201103723 – volume: 128 start-page: 78 year: 2006 ident: WOS:000234547700039 article-title: Palladium-catalyzed alkylation of aryl C-H bonds with sp(3) organotin reagents using benzoquinone as a crucial promoter publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja0570943 – volume: 202 start-page: C58 year: 1980 ident: WOS:A1980KU31400018 article-title: ALTERNATIVE SYNTHESIS OF ENANTIOMERIC 1-DIPHENYLPHOSPHINO-2-DIMETHYLAMINOMETHYLFERROCENE (KUMADAS LIGAND) publication-title: JOURNAL OF ORGANOMETALLIC CHEMISTRY – volume: 68 start-page: 4590 year: 2003 ident: WOS:000183066100070 article-title: Copper-catalyzed synthesis of unsymmetrical triarylphosphines publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo0343376 – volume: 662 start-page: 23 year: 2002 ident: WOS:000179271800004 article-title: Regioselective palladation of 2-oxazolinyl-[2.2]paracyclophanes. Synthesis of planar-chiral phosphines publication-title: JOURNAL OF ORGANOMETALLIC CHEMISTRY – volume: 7 start-page: 379 year: 2003 ident: WOS:000183051400025 article-title: Practical preparation and resolution of 1-(2 '-diphenylphosphino-1 '-naphthyl)isoquinoline: A useful ligand for catalytic asymmetric synthesis publication-title: ORGANIC PROCESS RESEARCH & DEVELOPMENT doi: 10.1021/op034007n – volume: 28 start-page: 1193 year: 2009 ident: WOS:000263420400035 article-title: Arylpalladium Phosphonate Complexes as Reactive Intermediates in Phosphorus-Carbon Bond Forming Reactions publication-title: ORGANOMETALLICS doi: 10.1021/om800906m – volume: 44 start-page: 941 year: 2012 ident: WOS:000301344200015 article-title: Direct Oxidative C-P Bond Formation of Indoles with Dialkyl Phosphites publication-title: SYNTHESIS-STUTTGART doi: 10.1055/s-0031-1289700 – volume: 9 start-page: 1407 year: 2007 ident: WOS:000245084300059 article-title: An efficient waste-free oxidative coupling via regioselective C-H bond cleavage: Rh/Cu-catalyzed reaction of benzoic acids with alkynes and acrylates under air publication-title: ORGANIC LETTERS doi: 10.1021/ol070406h – volume: 112 start-page: 3777 year: 2012 ident: WOS:000306298800004 article-title: Surface Modification Using Phosphonic Acids and Esters publication-title: CHEMICAL REVIEWS doi: 10.1021/cr2004212 – volume: 36 start-page: 1173 year: 2007 ident: WOS:000247341300014 article-title: Direct transition metal-catalyzed functionalization of heteroaromatic compounds publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/b606984n – volume: 28 start-page: 6546 year: 2009 ident: WOS:000271662700019 article-title: Reactions of Cyclopalladated Complexes with Lithium Diphenylphosphide publication-title: ORGANOMETALLICS doi: 10.1021/om9005615 – volume: 130 start-page: 16474 year: 2008 ident: WOS:000263320200016 article-title: Indole Synthesis via Rhodium Catalyzed Oxidative Coupling of Acetanilides and Internal Alkynes publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja806955s – volume: 35 start-page: 3484 year: 2002 ident: WOS:000175112100026 article-title: Phenylphosphonic acid functionalized poly [aryloxyphosphazenes] publication-title: MACROMOLECULES doi: 10.1021/ma0116295 – volume: 47 start-page: 6338 year: 2008 ident: WOS:000258584800004 article-title: Biaryl phosphane ligands in palladium-catalyzed amination publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION doi: 10.1002/anie.200800497 – volume: 59 start-page: 9471 year: 2003 ident: WOS:000186617600001 article-title: Chiral P,N-ligands with pyridine-nitrogen and phosphorus donor atoms. Syntheses and applications in asymmetric catalysis publication-title: TETRAHEDRON doi: 10.1016/j.tet.2003.09.066 – volume: 7 start-page: 477 year: 2003 ident: WOS:000181184000004 article-title: Catalytic synthesis of phosphines and related compounds publication-title: CURRENT ORGANIC CHEMISTRY – volume: 27 start-page: 5876 year: 2008 ident: WOS:000260791400017 article-title: Palladium-Catalyzed C-P Bond Formation: Mechanistic Studies on the Ligand Substitution and the Reductive Elimination. An Intramolecular Catalysis by the Acetate Group in Pd-II Complexes publication-title: ORGANOMETALLICS doi: 10.1021/om800641n – volume: 121 start-page: 6616 year: 1999 ident: WOS:000081603000010 article-title: Addition of olefins to aromatic ketones catalyzed by Rh(I) olefin complexes publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY – volume: 5 start-page: 2315 year: 2003 ident: WOS:000183692600031 article-title: Copper-catalyzed C-P bond construction via direct coupling of secondary phosphines and phosphites with aryl and vinyl halides publication-title: ORGANIC LETTERS doi: 10.1021/ol0346640 – volume: 77 start-page: 7706 year: 2012 ident: WOS:000308390100059 article-title: Coupling Reactions of Heteroarenes with Phosphites under Silver Catalysis publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo301108g – year: 2004 ident: 000321236600023.2 – volume: 366 start-page: 529 year: 1993 ident: WOS:A1993ML21800059 article-title: EFFICIENT CATALYTIC ADDITION OF AROMATIC CARBON-HYDROGEN BONDS TO OLEFINS publication-title: NATURE – volume: 10 start-page: 9627 year: 2012 ident: WOS:000311755100011 article-title: Nickel-catalyzed C-P cross-coupling of diphenylphosphine oxide with aryl chlorides publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c2ob26874d – volume: 55 start-page: 3837 year: 2012 ident: WOS:000303173600018 article-title: Structure-Guided Design, Synthesis, and Evaluation of Guanine-Derived Inhibitors of the eIF4E mRNA-Cap Interaction publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/jm300037x – volume: 79 start-page: 2217 year: 2007 ident: 000321236600023.26 publication-title: Pure Appl. Chem. – volume: 33 start-page: 336 year: 2000 ident: WOS:000087894400004 article-title: Phosphinooxazolines - A new class of versatile, modular P,N-ligands for asymmetric catalysis publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar9900865 – year: 2004 ident: 000321236600023.1 – volume: 54 start-page: 153 year: 2011 ident: WOS:000285818000012 article-title: Discovery of a Series of Phosphonic Acid-Containing Thiazoles and Orally Bioavailable Diamide Prodrugs That Lower Glucose in Diabetic Animals Through Inhibition of Fructose-1,6-Bisphosphatase publication-title: JOURNAL OF MEDICINAL CHEMISTRY – volume: 13 start-page: 3270 year: 2011 ident: WOS:000291409800076 article-title: Palladium-Catalyzed Cross-Coupling of H-Phosphinate Esters with Chloroarenes publication-title: ORGANIC LETTERS doi: 10.1021/ol201222n – volume: 49 start-page: 4682 year: 2013 ident: WOS:000318028500030 article-title: Palladium-catalyzed ortho-alkenylation of aryl hydrogen phosphates using a new mono-phosphoric acid directing group publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c3cc41107a – volume: 132 start-page: 9982 year: 2010 ident: WOS:000280227700019 article-title: Rh Catalyzed Olefination and Vinylation of Unactivated Acetanilides publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja103834b – volume: 111 start-page: 7981 year: 2011 ident: WOS:000297946600012 article-title: Review on Modern Advances of Chemical Methods for the Introduction of a Phosphonic Acid Group publication-title: CHEMICAL REVIEWS doi: 10.1021/cr2002646 – start-page: 56 year: 1981 ident: WOS:A1981KZ04900019 article-title: A NOVEL SYNTHESIS OF DIALKYL ARENEPHOSPHONATES publication-title: SYNTHESIS-STUTTGART – volume: 110 start-page: 1147 year: 2010 ident: WOS:000274705900016 article-title: Palladium-Catalyzed Ligand-Directed C-H Functionalization Reactions publication-title: CHEMICAL REVIEWS doi: 10.1021/cr900184e – volume: 68 start-page: 5130 year: 2012 ident: WOS:000305381700002 article-title: Challenges in C-C bond formation through direct transformations of sp(2) C-H bonds publication-title: TETRAHEDRON doi: 10.1016/j.tet.2012.05.040 – volume: 42 start-page: 1074 year: 2009 ident: WOS:000269308800009 article-title: Palladium- and Copper-Catalyzed Arylation of Carbon-Hydrogen Bonds publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar9000058 – volume: 45 start-page: 788 year: 2012 ident: WOS:000305321100003 article-title: Weak Coordination as a Powerful Means for Developing Broadly Useful C-H Functionalization Reactions publication-title: ACCOUNTS OF CHEMICAL RESEARCH doi: 10.1021/ar200185g – volume: 10 start-page: 3500 year: 2012 ident: WOS:000302420700017 article-title: Nickel-catalyzed C-P coupling of aryl mesylates and tosylates with H(O)(PRR2)-R-1 publication-title: ORGANIC & BIOMOLECULAR CHEMISTRY doi: 10.1039/c2ob25225b – volume: 76 start-page: 7370 year: 2011 ident: WOS:000294702000009 article-title: Palladium-Catalyzed Synthesis of Dibenzophosphole Oxides via Intramolecular Dehydrogenative Cyclization publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo201030j – volume: 132 start-page: 10565 year: 2010 ident: WOS:000280456100055 article-title: Rhodium-Catalyzed Oxidative Cycloaddition of Benzamides and Alkynes via C-H/N-H Activation publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja103776u – volume: 69 start-page: 5152 year: 2013 ident: WOS:000319647600013 article-title: Palladium(II)-catalyzed ortho-arylation via phosphate-group-directed C-H activation publication-title: TETRAHEDRON doi: 10.1016/j.tet.2013.04.067 – volume: 3 start-page: 2579 year: 2001 ident: WOS:000170392300041 article-title: Ruthenium complex-catalyzed direct ortho arylation and alkenylation of 2-arylpyridines with organic halides publication-title: ORGANIC LETTERS doi: 10.1021/ol016257z – volume: 123 start-page: 2685 year: 2001 ident: WOS:000167632900034 article-title: Annulation of alkenyl-substituted heterocycles via rhodium-catalyzed intramolecular C-H activated coupling reactions publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY – volume: 127 start-page: 2960 year: 2005 ident: WOS:000227479600050 article-title: Enantioselective esterification of prochiral phosphonate pendants of a polyphenylacetylene assisted by macromolecular helicity: Storage of a dynamic macromolecular helicity memory publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja042806v – volume: 36 start-page: 200 year: 2007 ident: WOS:000245866200001 article-title: Catalytic direct arylation of heteroaromatic compounds publication-title: CHEMISTRY LETTERS – volume: 15 start-page: 2186 year: 2013 ident: WOS:000318588900030 article-title: Pd(II)-Catalyzed ortho-Arylation of Aryl Phosphates and Aryl Hydrogen Phosphates with Diaryliodonium Triflates publication-title: ORGANIC LETTERS doi: 10.1021/ol400732q – volume: 103 start-page: 3029 year: 2003 ident: WOS:000184821500013 article-title: New chiral phosphorus ligands for enantioselective hydrogenation publication-title: CHEMICAL REVIEWS doi: 10.1021/cr020049i – volume: 128 start-page: 12634 year: 2006 ident: WOS:000240795000023 article-title: Palladium-catalyzed alkylation of sp(2) and sp(3) C-H bonds with methylboroxine and alkylboronic acids: Two distinct C-H activation pathways publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja0646747 – volume: 67 start-page: 5553 year: 2002 ident: WOS:000177318300013 article-title: Air stable, sterically hindered ferrocenyl dialkylphosphines for palladium-catalyzed C-C, C-N, and C-O bond-forming cross-couplings publication-title: JOURNAL OF ORGANIC CHEMISTRY doi: 10.1021/jo025732j – volume: 14 start-page: 2188 year: 2012 ident: WOS:000302990100061 article-title: Synthesis of Water-Soluble Phosphine Oxides by Pd/C-Catalyzed P-C Coupling in Water publication-title: ORGANIC LETTERS doi: 10.1021/ol300582y – start-page: 3037 year: 2010 ident: WOS:000282106400001 article-title: Transition-Metal-Catalyzed C-P Cross-Coupling Reactions publication-title: SYNTHESIS-STUTTGART doi: 10.1055/s-0030-1257960 – volume: 8 start-page: 407 year: 2006 ident: WOS:000235120700014 article-title: Phosphonation of arenes with dialkyl phosphites catalyzed by Mn(II)/CO(II)/O-2 redox couple publication-title: ORGANIC LETTERS doi: 10.1021/ol052406s – volume: 123 start-page: 337 year: 2001 ident: WOS:000166498600021 article-title: Ru-catalyzed oxidative coupling of arenes with olefins using O-2 publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja003361n – volume: 8 start-page: 5291 year: 2006 ident: WOS:000241729500029 article-title: Manganese(III) acetate promoted regioselective phosphonation of heteroaryl compounds publication-title: ORGANIC LETTERS doi: 10.1021/ol062082n – volume: 13 start-page: 2110 year: 2011 ident: WOS:000289187200056 article-title: Copper-Catalyzed C-P Bond Construction via Direct Coupling of Phenylboronic Acids with H-Phosphonate Diesters publication-title: ORGANIC LETTERS doi: 10.1021/ol200465z – volume: 117 start-page: 5371 year: 1995 ident: WOS:A1995QY88500025 article-title: ELABORATION OF CONJUGATED ALKENES INITIATED BY INSERTION INTO A VINYLIC C-H BOND publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY – volume: 45 start-page: 919 year: 2002 ident: WOS:000173985300018 article-title: New type of metalloproteinase inhibitor: Design and synthesis of new phosphonamide-based hydroxamic acids publication-title: JOURNAL OF MEDICINAL CHEMISTRY doi: 10.1021/jm0103211 – volume: 111 start-page: 1215 year: 2011 ident: WOS:000288820600003 article-title: Catalytic Dehydrogenative Cross-Coupling: Forming Carbon-Carbon Bonds by Oxidizing Two Carbon-Hydrogen Bonds publication-title: CHEMICAL REVIEWS doi: 10.1021/cr100280d – volume: 134 start-page: 9727 year: 2012 ident: WOS:000305107800032 article-title: General and Selective Copper-Catalyzed Reduction of Tertiary and Secondary Phosphine Oxides: Convenient Synthesis of Phosphines publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY doi: 10.1021/ja301764m – volume: 3 start-page: 4295 year: 2001 ident: WOS:000172939500043 article-title: Air-stable trialkylphosphonium salts: Simple, practical, and versatile replacements for air-sensitive trialkylphosphines. Applications in stoichiometric and catalytic processes publication-title: ORGANIC LETTERS doi: 10.1021/ol016971g – volume: 15 start-page: 13069 year: 2009 ident: WOS:000273697100021 article-title: Microwave-Promoted Palladium(II)-Catalyzed C-P Bond Formation by Using Arylboronic Acids or Aryltrifluoroborates publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.200901473 – volume: 48 start-page: 5181 year: 2012 ident: WOS:000303320000036 article-title: Palladium-catalyzed direct phosphonation of azoles with dialkyl phosphites publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c2cc30429e – volume: 351 start-page: 3207 year: 2009 ident: WOS:000273394500028 article-title: Preparation of Arylphosphonates by Palladium(0)-Catalyzed Cross-Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.200900590 – start-page: 63 year: 1999 ident: WOS:000078130200029 article-title: Isolation of the reactive intermediate in palladium-catalysed coupling of secondary phosphine-boranes with aryl halides publication-title: CHEMICAL COMMUNICATIONS – volume: 39 start-page: 3440 year: 2000 ident: WOS:000089732100015 article-title: The catalytic alkylation of aromatic imines by Wilkinson's complex: The domino reaction of hydroacylation and ortho-alkylation publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION |
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Snippet | A Pd(II)-catalyzed C–H phosphorylation reaction has been developed using heterocycle-directed ortho-palladation. Both H-phosphonates and diaryl phosphine... A Pd(II)-catalyzed C-H phosphorylation reaction has been developed using heterocycle-directed ortho-palladation. Both H-phosphonates and diaryl phosphine... |
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SubjectTerms | Catalysis chemical bonding Chemistry Chemistry, Multidisciplinary Molecular Structure Organometallic Compounds - chemistry Organophosphonates - chemistry oxides Oxides - chemistry Palladium - chemistry phosphine Phosphines - chemistry Phosphorylation Physical Sciences Pyridines - chemical synthesis Pyridines - chemistry Science & Technology |
Title | Pd(II)-Catalyzed Phosphorylation of Aryl C–H Bonds |
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