SAM 학술관계분석서비스

논문영향력 요약
주제	c?h activation functionalization palladium rhodium ruthenium
91	0	0.0%

논문영향력
주제	주제별 논문수	주제별 피인용횟수	주제별 논문영향력
주제어	c?h activation	4	0	0.0%
functionalization	32	0	0.0%
palladium	29	0	0.0%
rhodium	8	0	0.0%
ruthenium	19	0	0.0%
계		92	0	0.0%
* 다른 주제어 보유 논문에서 피인용된 횟수	0

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Huang, Y.-C.; Majumdar, K.K.; Cheng, C.-H. Nickel-catalyzed coupling of aryl iodides with aromatic aldehydes: Chemoselective synthesis of ketones. J. Org. Chem., 2002, 67, 1682-1684.

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For selected reviews of catalytic dehydrogenative cross-coupling reactions, see: a) C.-J. Li, Acc. Chem. Res. 2009, 42, 335; b) C. S. Yeung, V. M. Dong, Chem. Rev. 2011, 111, 1215.

For selected examples, see: (a) Z. Fu, S. Huang, W. Su and M. Hong, Org. Lett., 2010, 12, 4992; (b) P. Forgione, M. C. Brochu, M. St-Onge, K. H. Thesen, M. D. Bailey and F. Bilodeau, J. Am. Chem. Soc., 2006, 128, 11350.

For selected examples, see: (a) L. J. Goossen, N. Rodriguez and C. Linder, J. Am. Chem. Soc., 2008, 130, 15248; (b) L. J. Goossen, G. Deng and L. M. Levy, Science, 2006, 313, 662.

For selected examples, see: (a) F. Zhang and M. F. Greaney, Angew. Chem., Int. Ed., 2010, 49, 2768; (b) C. Wang, I. Piel and F. Glorius, J. Am. Chem. Soc., 2009, 131, 4194.

For selected examples on biological activities of phenylacetamide derivatives, see: (a) J. G. Samaritoni, L. Arndt, T. J. Bruce, J. E. Dripps, J. Gifford, C. J. Hatton, W. H. Hendrix, J. R. Schoonover, G. W. Johnson, V. B. Hegde and S. J. Thornburgh, Agric. Food Chem., 1997, 45, 1920; (b) P. K. Yonan, R. L. Novotney, C. M. Woo, K. A. Prodan, F. M. Hershenson, J. Med. Chem., 1980, 23, 1102; For selected examples on biological activities of phenylacetic acid derivatives, see: (c) W. R. Hudgins, S. Shack, C. E. Myers and D. Samid, Biochem. Pharmacol., 1995, 50, 1273; (d) H. Mart nez-Blanco, A. Reglero and J. M. Luengo, J. Ind. Microbiol., 1994, 13, 144.

For selected examples on C3-allylations, see: (a) Butsugan, Y.; Nagai, K.; Nagaya, F.; Tabuchi, H.; Yamada, K.; Araki, S. Bull. Chem. Soc. Jpn. 1988, 61, 1707. (b) Zhu, X.; Ganesan, A. J. Org. Chem. 2002, 67, 2705. (c) McCubbin, J. A.; Hosseini, H.; Krokhin, O. V. J. Org. Chem. 2010, 75, 959. (d) Kimura, M.; Futamata, M.; Mukai, R.; Tamaru, Y. J. Am. Chem. Soc. 2005, 127, 4592. (e) Ma, S.; Yu, S.; Peng, Z.; Guo, H. J. Org. Chem. 2006, 71, 9865. (f) Zaitsev, A. B.; Gruber, S.; Pl ss, P. A.; Pregosin, P. S.; Veiros, L. F.; W rle, M. J. Am. Chem. Soc. 2008, 130, 11604. (g) Sundararaju, B.; Achard, M.; Demerseman, B.; Toupet, L.; Sharma, G. V. M.; Bruneau, C. Angew. Chem., Int. Ed. 2010, 49, 2782. (h) Montgomery, T. D.; Zhu, Y.; Kagawa, N.; Rawal, V. H. Org. Lett. 2013, 15, 1140.

For selected examples on C2-allylations, see: (a) Gagnon, D.; Spino, C. J. Org. Chem. 2009, 74, 6035. (b) Yamakawa, T.; Ideue, E.; Shimokawa, J.; Fukuyama, T. Angew. Chem., Int. Ed. 2010, 49, 9262. (c) Auzzas, L.; Larsson, A.; Matera, R.; Baraldi, A.; Desch nes-Simard, B.; Giannini, G.; Cabri, W.; Battistuzzi, G.; Gallo, G.; Ciacci, A.; Vesci, L.; Pisano, C.; Hanessian, S. J. Med. Chem. 2010, 53, 8387. (d) Bennasar, M.; Sol , D.; Zulaica, E.; Alonso, S. Org. Lett. 2011, 13, 2042. (e) Li, B.; Ma, J.; Xie, W.; Song, H.; Xu, S.; Wang, B. Chem.–Eur. J. 2013, 19, 11863. (f) Kim, M.; Park, J.; Sharma, S.; Han, S.; Han, S. H.; Kwak, J. H.; Jung, Y. H.; Kim, I. S. Org. Biomol. Chem. 2013, 11, 7427.

For recent selected examples, see: (a) Zhao, X.; Dimitrijević, E.; Dong, V. M. J. Am. Chem. Soc. 2009, 131, 3466–3467. (b) Wang, X.; Mei, T.-S.; Yu, J.-Q. J. Am. Chem. Soc. 2009, 131, 7520–7521. (c) Mei, T.-S.; Giri, R.; Maugel, N.; Yu, J.-Q. Angew. Chem. Int. Ed. 2008, 47, 5215–5219. (d) Li, J.-J.; Mei, T.-S.; Yu, J.-Q. Angew. Chem. Int. Ed. 2008, 47, 6452–6455. (e) Hull, K. L.; Anani, W. Q.; Sanford, M. S. J. Am. Chem. Soc. 2006, 128, 7134–7135.

For recent selected examples, see: (a) Zhao, X.; Dimitrijević, E.; Dong, V. M. J. Am. Chem. Soc. 2009, 131, 3466. (b) Wang, X.; Mei, T.-S.; Yu, J.-Q. J. Am. Chem. Soc. 2009, 131, 7520.

For recent selected examples, see: (a) Wang, X.; Lu, Y.; Dai, H.-X.; Yu, J.-Q. J. Am. Chem. Soc. 2010, 132, 12203–12205. (b) Zhang, Y.-H.; Yu, J.-Q. J. Am. Chem. Soc. 2009, 131, 14654–14655. (c) Powers, D. C.; Geibel, M. A. L.; Klein, J. E. M. N.; Ritter, T. J. Am. Chem. Soc. 2009, 131, 17050–17051. (d) Desai, L. V.; Stowers, K. J.; Sanford, M. S. J. Am. Chem. Soc. 2008, 130, 13285–13293.

For recent selected examples, see: (a) Wang, X.; Lu, Y.; Dai, H.-X.; Yu, J.-Q. J. Am. Chem. Soc. 2010, 132, 12203. (b) Zhang, Y.-H.; Yu, J.-Q. J. Am. Chem. Soc. 2009, 131, 14654.

For recent selected examples, see: (a) Muralirajan, K.; Parthasarathy, K.; Cheng, C.-H. Angew. Chem. Int. Ed. 2011, 50, 4169–4172. (b) Rakshit, S.; Patureau, F. W.; Glorius, F. J. Am. Chem. Soc. 2010, 132, 9585–9587. (c) Guimond, N.; Gouliaras, C.; Fagnou, K. J. Am. Chem. Soc. 2010, 132, 6908–6909. (d) Morimoto, K.; Hirano, K.; Satoh, T.; Miura, M. Org. Lett. 2010, 12, 2068–2071. (e) Mochida, S.; Hirano, K.; Satoh, T.; Miura, M. J. Org. Chem. 2009, 74, 6295–6298. (f) Guimond, N.; Fagnou, K. J. Am. Chem. Soc. 2009, 131, 12050–12051. (g) Li, L.; Brennessel, W. W.; Jones, W. D. J. Am. Chem. Soc. 2008, 130, 12414–12419. (h) Umeda, N.; Tsurugi, H.; Satoh, T.; Miura, M. Angew. Chem. Int. Ed. 2008, 47, 4019–4022. (i) Stuart, D. R.; Bertrand-Laperle, M.; Burgess, K. M. N.; Fagnou, K. J. Am. Chem. Soc. 2008, 130, 16474–16475.

For recent selected examples, see: (a) Muralirajan, K.; Parthasarathy, K.; Cheng, C.-H. Angew. Chem. Int. Ed. 2011, 50, 4169. (b) Lu, Y.; Wang, D.-H.; Engle, K. M.; Yu, J.-Q. J. Am. Chem. Soc. 2010, 132, 5916. (c) Xiao, B.; Fu, Y.; Xu, J.; Gong, T.-J.; Dai, J.-J.; Yi, J.; Liu, L. J. Am. Chem. Soc. 2010, 132, 468. (d) Patureau, F. W.; Glorius, F. J. Am. Chem. Soc. 2010, 132, 9982. (e) Wang, D.-H.; Engle, K. M.; Shi, B.-F.; Yu, J.-Q. Science 2010, 327, 315. (f) Guimond, N.; Gouliaras, C.; Fagnou, K. J. Am. Chem. Soc. 2010, 132, 6908.

For recent selected examples, see: (a) Lu, Y.; Wang, D.-H.; Engle, K. M.; Yu, J.-Q. J. Am. Chem. Soc. 2010, 132, 5916–5921. (b) Schiffner, J. A.; W ste, T. H.; Oestreich, M. Eur. J. Org. Chem. 2010, 174–182. (c) Xiao, B.; Fu, Y.; Xu, J.; Gong, T.-J.; Dai, J.-J.; Yi, J.; Liu, L. J. Am. Chem. Soc. 2010, 132, 468–469. (d) Patureau, F. W.; Glorius, F. J. Am. Chem. Soc. 2010, 132, 9982–9983. (e) Wang, D.-H.; Engle, K. M.; Shi, B.-F.; Yu, J.-Q. Science 2010, 327, 315-319. (f) Wasa, M.; Engle, K. M.; Yu, J.-Q. J. Am. Chem. Soc. 2010, 132, 3680–3681. (g) Wang, F.; Song, G.; Li, X. Org. Lett. 2010, 12, 5430–5433. (h) Zhang, Y.-H.; Shi, B.-F.; Yu, J.-Q. J. Am. Chem. Soc. 2009, 131, 5072–5074. (i) Garc a-Rubia, A.; Array s, R. G.; Carretero, J. C. Angew. Chem. Int. Ed. 2009, 48, 6511–6515.

For recent selected examples, see: (a) Cho, S. H.; Yoon, J.; Chang, S. J. Am. Chem. Soc. 2011, 133, 5996. (b) Ackermann, L.; Lygin, A. V.; Hofmann, N. Org. Lett. 2011, 13, 3278.

For recent selected examples, see: (a) Ackermann, L.; Lygin, A. V.; Hofmann, N. Org. Lett. 2011, 13, 3278–3281. (b) Cho, S. H.; Yoon, J.; Chang, S. J. Am. Chem. Soc. 2011, 133, 5996–6005. (c) Shuai, Q.; Deng, G.; Chua, J.; Bohle, D. S.; Li, C.-J. Adv. Synth. Cat. 2010, 352, 632–636. (d) Mei, T.-S.; Wang, X.; Yu, J.-Q. J. Am. Chem. Soc. 2009, 131, 10806–10807. (e) Wang, Q.; Schreiber, S. L. Org. Lett. 2009, 11, 5178–5180. (f) Monguchi, D.; Fujiwara, T.; Furukawa, H.; Mori, A. Org. Lett. 2009, 11, 1607–1610.

For recent reviews, see: (a) J. Cornella and I. Larrosa, Synthesis, 2012, 44, 653; (b) N. Rodriguez and L. J. Goossen, Chem. Soc. Rev., 2011, 40, 5030.

For recent reviews on catalytic dehydrogenative cross-coupling, see: a) C. S. Yeung, V. M. Dong, Chem. Rev. 2011, 111, 1215; b) C.-J. Li, Acc. Chem. Res. 2009, 42, 335; c) C. J. Scheuermann, Chem.—Asian. J. 2010, 5, 436.

For recent reviews on C–H functionalization, see: a) L. Ackermann, Chem. Rev. 2011, 111, 1315; b) S. H. Cho, J. Y. Kim, J. Kwak, S. Chang, Chem. Soc. Rev. 2011, 40, 5068; c) J. Wencel-Delord, T. Dr ge, F. Kiu, F. Glorius, Chem. Soc. Rev. 2011, 40, 4740; d) O. Baudoin, Chem. Soc. Rev. 2011, 40, 4902; e) L. McMurray, F. O’Hara, M. J. Gaunt, Chem. Soc. Rev. 2011, 40, 1885; f) J. L. Bras, J. Muzart, Chem. Rev. 2011, 111, 1170; g) T. W. Lyons, M. S. Sanford, Chem. Rev. 2010, 110, 1147; h) I. A. I. Mkhalid, J. H. Barnard, T. B. Marder, J. M. Murphy, J. F. Hartwig, Chem. Rev. 2010, 110, 890; i) C. Cop ret, Chem. Rev. 2010, 110, 656; j) D. A. Colby, R. G. Bergmann, J. A. Ellman, 2010, 110, 624; l) J. Q. Yu, Z. J. Shi in C–H Activation; Springer: Berlin, Germany, 2010.

For recent reviews on C–H bond functionalization, see: (a) Wencel-Delord, J.; Dr ge, T.; Liu, F.; Glorius, F. Chem. Soc. Rev. 2011, 40, 4740. (b) Ackermann, L. Chem. Rev. 2011, 111, 1315. (c) Mkhalid, I. A. I.; Barnard, J. H.; Marder, T. B.; Murphy, J. M.; Hartwig, J. F. Chem. Rev. 2010, 110, 890. (d) Cop ret, C. Chem. Rev. 2010, 110, 656. (e) Colby, D. A.; Bergman, R. G.; Ellman, J. A. Chem. Rev. 2010, 110, 624. (f) Beck, E. M.; Gaunt, M. J. Top. Curr. Chem. 2010, 292, 85.

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For recent reviews on C–H bond activation, see: (a) L. Ackermann, Chem. Rev., 2011, 111, 1315; (b) S. H. Cho, J. Y. Kim, J. Kwak and S. Chang, Chem. Soc. Rev., 2011, 40, 5068; (c) J. Wencel-Delord, T. Dr ge, F. Liu and F. Glorius, Chem. Soc. Rev., 2011, 40, 4740; (d) O. Baudoin, Chem. Soc. Rev., 2011, 40, 4902; (e) J. L. Bras and J. Muzart, Chem. Rev., 2011, 111, 1170.

For recent reviews on C–C cross coupling reactions, see: (a) J. Magano and J. R. Dunetz, Chem. Rev., 2011, 111, 2177; (b) N. Rodriguez and L. J. Goossen, Chem. Soc. Rev., 2011, 40, 5030; (c) G. C. Fortman and S. P. Nolan, Chem. Soc. Rev., 2011, 40, 5151; (d) C. Liu, H. Zhang, W. Shi and A. Lei, Chem. Rev., 2011, 111, 1780.

For ortho-iodination and alkenylation of N-benzyltriflamides, see: (a) X. Wang, T.-S. Mei and J.-Q. Yu, J. Am. Chem. Soc., 2009, 131, 7520.

For detailed mechanistic studies of Rh(III)-catalyzed C–H bond functionalization, see: (a) Stuart, D. R.; Bertrand-Laperle, M.; Burgess, K. M. N.; Fagnou, K. J. Am. Chem. Soc. 2008, 130, 16474. (b) Stuart, D. R.; Alsaben, P.; Kuhn, M.; Fagnou, K. J. Am. Chem. Soc. 2010, 132, 18326.

For benzylic oxidation using TBHP, see: a) G. Rothenberg, L. Feldberg, H. Wiener, Y. Sasson, J. Chem. Soc., Perkin. Trans. 2 1998, 2429; b) M. Nakanishi, C. Bolm, Adv. Synth. Catal. 2007, 349, 861; c) C. S. Yi, K.-H. Kwon, D. W. Lee, Org. Lett. 2009, 11, 1567; d) R. A. Kumar, C. U. Maheswari, S. Ghantasala, C. Jyothi, K. R. Reddy, Adv. Synth. Catal. 2011, 353, 401; e) S. Nawratil, M. Grypioti, C. Menendez, S. Mallet-Ladeira, C. Lherbet, M. Baltas, Eur. J. Org. Chem. 2013, 654.

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For a review of acyl radicals, see: (a) C. Chatgilialoglu, D. Crich, M. Komatsu and I. Ryu, Chem. Rev., 1999, 99, 1991; For recent selected examples of acyl radicals, see: (b) Z. Shi and F. Glorius, Chem. Sci., 2013, 4, 829; (c) Z. Liu, J. Zhang, S. Chen, E. Shi, Y. Xu and X. Wan, Angew. Chem., Int. Ed., 2012, 51, 3231.

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