참고문헌 (63)

1. Nat. Chem. Biol. R Hili 2 284 2006 10.1038/nchembio0606-284 Hili, R. & Yudin, A. K. Making carbon-nitrogen bonds in biological and chemical synthesis. Nat. Chem. Biol. 2, 284-287 (2006). 

   상세보기

2. 10.1002/9783527621262 Ricci, A. Amino Group Chemistry: from Synthesis to the Life Sciences (Wiley, 2008). 

   

3. J. Nat. Prod. LM Blair 76 794 2013 10.1021/np400124n Blair, L. M. & Sperry, J. Natural products containing a nitrogen-nitrogen bond. J. Nat. Prod. 76, 794-812 (2013). 

   상세보기

4. Chem. Rev. AJ Waldman 117 5784 2017 10.1021/acs.chemrev.6b00621 Waldman, A. J., Ng, T. L., Wang, P. & Balskus, E. P. Heteroatom-heteroatom bond formation in natural product biosynthesis. Chem. Rev. 117, 5784-5863 (2017). 

   상세보기

5. Chem. Soc. Rev. U Ragnarsson 30 205 2001 10.1039/b010091a Ragnarsson, U. Synthetic methodology for alkyl substituted hydrazines. Chem. Soc. Rev. 30, 205-213 (2001). 

   상세보기

6. Synthesis QH Guo 49 3835 2017 10.1055/s-0036-1588512 Guo, Q. H. & Lu, Z. Recent advances in nitrogen-nitrogen bond formation. Synthesis 49, 3835-3847 (2017). 

   상세보기

7. Org. Lett. M Wolter 3 3803 2001 10.1021/ol0168216 Wolter, M., Klapars, A. & Buchwald, S. L. Synthesis of N-aryl hydrazides by copper-catalyzed coupling of hydrazides with aryl iodides. Org. Lett. 3, 3803-3805 (2001). 

   상세보기

8. Org. Lett. DA Evans 1 595 1999 10.1021/ol990113r Evans, D. A. & Johnson, D. S. Catalytic enantioselective amination of enolsilanes using C2-symmetric copper(ii) complexes as chiral Lewis acids. Org. Lett. 1, 595-598 (1999). 

   상세보기

9. Tetrahedron Lett. J Vidal 39 8845 1998 10.1016/S0040-4039(98)01983-2 Vidal, J., Hannachi, J. C., Hourdin, G., Mulatier, J. C. & Collet, A. N-Boc-3-trichloromethyloxaziridine: a new, powerful reagent for electrophilic amination. Tetrahedron Lett. 39, 8845-8848 (1998). 

   상세보기

10. J. Am. Chem. Soc. BR Rosen 136 5571 2014 10.1021/ja5013323 Rosen, B. R., Werner, E. W., O’Brien, A. G. & Baran, P. S. Total synthesis of dixiamycin B by electrochemical oxidation. J. Am. Chem. Soc. 136, 5571-5574 (2014). 

    상세보기

11. J. Am. Chem. Soc. MC Ryan 140 9074 2018 10.1021/jacs.8b05245 Ryan, M. C., Martinelli, J. R. & Stahl, S. S. Cu-catalyzed aerobic oxidative N-N coupling of carbazoles and diarylamines including selective cross-coupling. J. Am. Chem. Soc. 140, 9074-9077 (2018). 

    상세보기

12. Chem. Sci. MC Ryan 11 1170 2020 10.1039/C9SC04305E Ryan, M. C. et al. Mechanistic insights into copper-catalyzed aerobic oxidative coupling of N-N bonds. Chem. Sci. 11, 1170-1175 (2020). 

    상세보기

13. Org. Lett. BJ Stokes 12 2884 2010 10.1021/ol101040p Stokes, B. J., Vogel, C. V., Urnezis, L. K., Pan, M. & Driver, T. G. Intramolecular Fe(ii)-catalyzed N-O or N-N bond formation from aryl azides. Org. Lett. 12, 2884-2887 (2010). 

    상세보기

14. Angew. Chem. Int. Ed. JJ Neumann 49 7790 2010 10.1002/anie.201002389 Neumann, J. J., Suri, M. & Glorius, F. Efficient synthesis of pyrazoles: oxidative C-C/N-N bond-formation cascade. Angew. Chem. Int. Ed. 49, 7790-7794 (2010). 

    상세보기

15. Org. Lett. Y Zhang 21 4960 2019 10.1021/acs.orglett.9b01396 Zhang, Y. et al. Fe(iii)-catalyzed aerobic intramolecular N-N coupling of aliphatic azides with amines. Org. Lett. 21, 4960-4965 (2019). 

    상세보기

16. Angew. Chem. Int. Ed. JB Diccianni 55 7534 2016 10.1002/anie.201602566 Diccianni, J. B., Hu, C. H. & Diao, T. N. N-N bond forming reductive elimination via a mixed-valent nickel(ii)-nickel(iii) intermediate. Angew. Chem. Int. Ed. 55, 7534-7538 (2016). 

    상세보기

17. J. Am. Chem. Soc. L Maestre 139 2216 2017 10.1021/jacs.6b08219 Maestre, L. et al. Functional-group-tolerant, silver-catalyzed N-N bond formation by nitrene transfer to amines. J. Am. Chem. Soc. 139, 2216-2223 (2017). 

    상세보기

18. Nat. Chem. J Li 5 634 2013 10.1038/nchem.1685 Li, J. et al. Erratum: Simultaneous structure-activity studies and arming of natural products by C-H amination reveal cellular targets of eupalmerin acetate. Nat. Chem. 5, 634-634 (2013). 

    상세보기

19. Chem. Eur. J. M Kono 25 3119 2019 10.1002/chem.201805878 Kono, M., Harada, S. & Nemoto, T. Chemoselective intramolecular formal insertion reaction of Rh-nitrenes into an amide bond over C-H insertion. Chem. Eur. J. 25, 3119-3124 (2019). 

    상세보기

20. 10.1002/9783527342822.ch8 Dehghany, M., Eshon, J., Roberts, J. M. & Schomaker, J. M. in Silver Catalysis in Organic Synthesis (eds Li, C. J. & Bi, X. H.) Ch. 8, 439-532 (Wiley, 2019). 

    

21. J. Am. Chem. Soc. K Lang 141 12388 2019 10.1021/jacs.9b05850 Lang, K., Torker, S., Wojtas, L. & Zhang, X. P. Asymmetric induction and enantiodivergence in catalytic radical C-H amination via enantiodifferentiative H-atom abstraction and stereoretentive radical substitution. J. Am. Chem. Soc. 141, 12388-12396 (2019). 

    상세보기

22. Nat. Catal. M Ju 2 899 2019 10.1038/s41929-019-0339-y Ju, M. et al. Tunable catalyst-controlled syntheses of β- and γ-amino alcohols enabled by silver-catalysed nitrene transfer. Nat. Catal. 2, 899-908 (2019). 

    상세보기

23. Nature HML Davies 451 417 2008 10.1038/nature06485 Davies, H. M. L. & Manning, J. R. Catalytic C-H functionalization by metal carbenoid and nitrenoid insertion. Nature 451, 417-424 (2008). 

    상세보기

24. J. Am. Chem. Soc. Y Park 138 14020 2016 10.1021/jacs.6b08211 Park, Y., Heo, J., Baik, M.-H. & Chang, S. Why is the Ir(iii)-mediated amido transfer much faster than the Rh(iii)-mediated reaction? A combined experimental and computational study. J. Am. Chem. Soc. 138, 14020-14029 (2016). 

    상세보기

25. Chem. Rev. Y Park 117 9247 2017 10.1021/acs.chemrev.6b00644 Park, Y., Kim, Y. & Chang, S. Transition metal-catalyzed C-H amination: scope, mechanism and applications. Chem. Rev. 117, 9247-9301 (2017). 

    상세보기

26. Science SY Hong 359 1016 2018 10.1126/science.aap7503 Hong, S. Y. et al. Selective formation of γ-lactams via C-H amidation enabled by tailored iridium catalysts. Science 359, 1016-1021 (2018). 

    상세보기

27. J. Am. Chem. Soc. Y Park 137 4534 2015 10.1021/jacs.5b01324 Park, Y., Park, K. T., Kim, J. G. & Chang, S. Mechanistic studies on the Rh(iii)-mediated amido transfer process leading to robust C-H amination with a new type of amidating reagent. J. Am. Chem. Soc. 137, 4534-4542 (2015). 

    상세보기

28. Angew. Chem. Int. Ed. G Dequirez 51 7384 2012 10.1002/anie.201201945 Dequirez, G., Pons, V. & Dauban, P. Nitrene chemistry in organic synthesis: still in its infancy? Angew. Chem. Int. Ed. 51, 7384-7395 (2012). 

    상세보기

29. Chem. Eur. J. T Shimbayashi 25 3156 2019 10.1002/chem.201803716 Shimbayashi, T., Sasakura, K., Eguchi, A., Okamoto, K. & Ohe, K. Recent progress on cyclic nitrenoid precursors in transition-metal-catalyzed nitrene-transfer reactions. Chem. Eur. J. 25, 3156-3180 (2019). 

    상세보기

30. ACS Catal. KM van Vliet 10 4751 2020 10.1021/acscatal.0c00961 van Vliet, K. M. & de Bruin, B. Dioxazolones: stable substrates for the catalytic transfer of acyl nitrenes. ACS Catal. 10, 4751-4769 (2020). 

    상세보기

31. Tetrahedron Lett. J Sauer 9 319 1968 10.1016/S0040-4039(01)98753-2 Sauer, J. & Mayer, K. K. Thermolyse und photolyse von 3-subtituierten Δ2-1.4.2-dioxazolinonen-(5), Δ2-1.4.2-dioxazolin-thionen-(5) und 4-substituierten Δ3-1.2.5.3-thiadioxazolin-s-oxiden. Tetrahedron Lett. 9, 319-324 (1968). 

    상세보기

32. Angew. Chem. Int. Ed. V Bizet 53 5639 2014 10.1002/anie.201310790 Bizet, V., Buglioni, L. & Bolm, C. Light-induced ruthenium-catalyzed nitrene transfer reactions: a photochemical approach towards N-acyl sulfimides and sulfoximines. Angew. Chem. Int. Ed. 53, 5639-5642 (2014). 

    상세보기

33. Angew. Chem. Int. Ed. H Lebel 53 7300 2014 10.1002/anie.201402961 Lebel, H., Piras, H. & Bartholomeus, J. Rhodium-catalyzed stereoselective amination of thioethers with N-mesyloxycarbamates: DMAP and bis(DMAP)CH2Cl2 as key additives. Angew. Chem. Int. Ed. 53, 7300-7304 (2014). 

    상세보기

34. J. Am. Chem. Soc. KM van Vliet 141 15240 2019 10.1021/jacs.9b07140 van Vliet, K. M. et al. Efficient copper-catalyzed multicomponent synthesis of N-acyl amidines via acyl nitrenes. J. Am. Chem. Soc. 141, 15240-15249 (2019). 

    상세보기

35. Nat. Catal. Y Park 2 219 2019 10.1038/s41929-019-0230-x Park, Y. & Chang, S. Asymmetric formation of γ-lactams via C-H amidation enabled by chiral hydrogen-bond-donor catalysts. Nat. Catal. 2, 219-227 (2019). 

    상세보기

36. J. Am. Chem. Soc. H Wang 141 7194 2019 10.1021/jacs.9b02811 Wang, H. et al. Iridium-catalyzed enantioselective C(sp3)-H amidation controlled by attractive noncovalent interactions. J. Am. Chem. Soc. 141, 7194-7201 (2019). 

    상세보기

37. J. Am. Chem. Soc. Q Xing 141 3849 2019 10.1021/jacs.9b00535 Xing, Q., Chan, C. M., Yeung, Y. W. & Yu, W. Y. Ruthenium(ii)-catalyzed enantioselective γ-lactams formation by intramolecular C-H amidation of 1,4,2-dioxazol-5-ones. J. Am. Chem. Soc. 141, 3849-3853 (2019). 

    상세보기

38. Acc. Chem. Res. JL Roizen 45 911 2012 10.1021/ar200318q Roizen, J. L., Harvey, M. E. & Du Bois, J. Metal-catalyzed nitrogen-atom transfer methods for the oxidation of aliphatic C-H bonds. Acc. Chem. Res. 45, 911-922 (2012). 

    상세보기

39. Angew. Chem. Int. Ed. H Wang 54 13049 2015 10.1002/anie.201506323 Wang, H., Tang, G. & Li, X. Rhodium(iii)-catalyzed amidation of unactivated C(sp3)-H bonds. Angew. Chem. Int. Ed. 54, 13049-13052 (2015). 

    상세보기

40. ACS Catal. R Mei 6 793 2016 10.1021/acscatal.5b02661 Mei, R., Loup, J. & Ackermann, L. Oxazolinyl-assisted C-H amidation by cobalt(iii) catalysis. ACS Catal. 6, 793-797 (2016). 

    상세보기

41. J. Am. Chem. Soc. H Lei 141 2268 2019 10.1021/jacs.9b00237 Lei, H. & Rovis, T. Ir-catalyzed intermolecular branch-selective allylic C-H amidation of unactivated terminal olefins. J. Am. Chem. Soc. 141, 2268-2273 (2019). 

    상세보기

42. Angew. Chem. Int. Ed. T Knecht 58 7117 2019 10.1002/anie.201901733 Knecht, T., Mondal, S., Ye, J. H., Das, M. & Glorius, F. Intermolecular, branch-selective, and redox-neutral Cp*Ir(iii)-catalyzed allylic C-H amidation. Angew. Chem. Int. Ed. 58, 7117-7121 (2019). 

    상세보기

43. Angew. Chem. Int. Ed. RJ Scamp 59 890 2020 10.1002/anie.201911886 Scamp, R. J., deRamon, E., Paulson, E. K., Miller, S. J. & Ellman, J. A. Co(iii)-catalyzed C-H amidation of dehydroalanine for the site-selective structural diversification of thiostrepton. Angew. Chem. Int. Ed. 59, 890-895 (2020). 

    상세보기

44. J. Am. Chem. Soc. Z Zhou 141 19048 2019 10.1021/jacs.9b09301 Zhou, Z. et al. Non-C2-symmetric chiral-at-ruthenium catalyst for highly efficient enantioselective intramolecular C(sp3)-H amidation. J. Am. Chem. Soc. 141, 19048-19057 (2019). 

    상세보기

45. ACS Catal. JS Burman 9 5474 2019 10.1021/acscatal.9b01338 Burman, J. S., Harris, R. J., B. Farr, C. M., Bacsa, J. & Blakey, S. B. Rh(iii) and Ir(iii)Cp* complexes provide complementary regioselectivity profiles in intermolecular allylic C-H amidation reactions. ACS Catal. 9, 5474-5479 (2019). 

    상세보기

46. Angew. Chem. Int. Ed. PW Tan 56 16550 2017 10.1002/anie.201709273 Tan, P. W., Mak, A. M., Sullivan, M. B., Dixon, D. J. & Seayad, J. Thioamide-directed cobalt(iii)-catalyzed selective amidation of C(sp3)−H bonds. Angew. Chem. Int. Ed. 56, 16550-16554 (2017). 

    상세보기

47. Angew. Chem. Int. Ed. S Fukagawa 58 18154 2019 10.1002/anie.201911268 Fukagawa, S., Kojima, M., Yoshino, T. & Matsunaga, S. Catalytic enantioselective methylene C(sp3)-H amidation of 8-alkylquinolines using a Cp*Rhiii/chiral carboxylic acid system. Angew. Chem. Int. Ed. 58, 18154-18158 (2019). 

    상세보기

48. Org. Lett. P Dube 11 5622 2009 10.1021/ol9023387 Dube, P. et al. Carbonyldiimidazole-mediated Lossen rearrangement. Org. Lett. 11, 5622-5625 (2009). 

    상세보기

49. Angew. Chem. Int. Ed. L Legnani 55 2248 2016 10.1002/anie.201507630 Legnani, L. & Morandi, B. Direct catalytic synthesis of unprotected 2-amino-1-phenylethanols from alkenes by using iron(ii) phthalocyanine. Angew. Chem. Int. Ed. 55, 2248-2251 (2016). 

    상세보기

50. J. Am. Chem. Soc. G-S Liu 135 3343 2013 10.1021/ja311923z Liu, G.-S., Zhang, Y.-Q., Yuan, Y.-A. & Xu, H. Iron(ii)-catalyzed intramolecular aminohydroxylation of olefins with functionalized hydroxylamines. J. Am. Chem. Soc. 135, 3343-3346 (2013). 

    상세보기

51. Org. Lett. Y-Q Zhang 15 3910 2013 10.1021/ol401666e Zhang, Y.-Q., Yuan, Y.-A., Liu, G.-S. & Xu, H. Iron(ii)-catalyzed asymmetric intramolecular aminohydroxylation of indoles. Org. Lett. 15, 3910-3913 (2013). 

    상세보기

52. Org. Lett. Y Zhang 21 4960 2019 10.1021/acs.orglett.9b01396 Zhang, Y. et al. Fe(iii)-catalyzed aerobic intramolecular N−N coupling of aliphatic azides with amines. Org. Lett. 21, 4960-4965 (2019). 

    상세보기

53. Angew. Chem. Int. Ed. H Yu 57 12053 2018 10.1002/anie.201804284 Yu, H., Li, Z. & Bolm, C. Three-dimensional heterocycles by iron-catalyzed ring-closing sulfoxide imidation. Angew. Chem. Int. Ed. 57, 12053-12056 (2018). 

    상세보기

54. Org. Biomol. Chem. J Yao 12 5469 2014 10.1039/c4ob00921e Yao, J., Feng, R., Lin, C., Liu, Z. & Zhang, Y. Synthesis of 2,3-dihydro-1H-indazoles by Rh(iii)-catalyzed C-H cleavage of arylhydrazines. Org. Biomol. Chem. 12, 5469-5476 (2014). 

    상세보기

55. Org. Lett. S Han 16 2494 2014 10.1021/ol500865j Han, S. et al. Rh(iii)-catalyzed oxidative coupling of 1,2-disubstituted arylhydrazines and olefins: a new strategy for 2,3-dihydro-1H-indazoles. Org. Lett. 16, 2494-2497 (2014). 

    상세보기

56. Angew. Chem. Int. Ed. F Zhan 52 1266 2013 10.1002/anie.201207173 Zhan, F. & Liang, G. Formation of enehydrazine intermediates through coupling of phenylhydrazines with vinyl halides: entry into the Fischer indole synthesis. Angew. Chem. Int. Ed. 52, 1266-1269 (2013). 

    상세보기

57. Angew. Chem. Int. Ed. FW Patureau 50 1977 2011 10.1002/anie.201007241 Patureau, F. W. & Glorius, F. Oxidizing directing groups enable efficient and innovative C-H activation reactions. Angew. Chem. Int. Ed. 50, 1977-1979 (2011). 

    상세보기

58. J. Comput. Chem. T Lu 33 580 2012 10.1002/jcc.22885 Lu, T. & Chen, F. Multiwfn: a multifunctional wavefunction analyzer. J. Comput. Chem. 33, 580-592 (2012). 

    상세보기

59. J. Am. Chem. Soc. SM Rummelt 137 5506 2015 10.1021/jacs.5b01475 Rummelt, S. M., Radkowski, K., Rosca, D. A. & Furstner, A. Interligand interactions dictate the regioselectivity of trans-hydrometalations and related reactions catalyzed by [Cp*RuCl]. hydrogen bonding to a chloride ligand as a steering principle in catalysis. J. Am. Chem. Soc. 137, 5506-5519 (2015). 

    상세보기

60. Chem. Eur. J. PF Kuijpers 23 13819 2017 10.1002/chem.201702537 Kuijpers, P. F., van der Vlugt, J. I., Schneider, S. & de Bruin, B. Nitrene radical intermediates in catalytic synthesis. Chem. Eur. J. 23, 13819-13829 (2017). 

    상세보기

61. Science ET Hennessy 340 591 2013 10.1126/science.1233701 Hennessy, E. T. & Betley, T. A. Complex N-heterocycle synthesis via iron-catalyzed, direct C-H bond amination. Science 340, 591-595 (2013). 

    상세보기

62. Angew. Chem. Int. Ed. K-P Shing 57 11947 2018 10.1002/anie.201806059 Shing, K.-P. et al. N-heterocyclic carbene iron(iii) porphyrin-catalyzed intramolecular C(sp3)-H amination of alkyl azides. Angew. Chem. Int. Ed. 57, 11947-11951 (2018). 

    상세보기

63. Chin. J. Chem. P Wang 36 1222 2018 10.1002/cjoc.201800427 Wang, P. & Deng, L. Recent advances in iron-catalyzed C-H bond amination via iron imido intermediate. Chin. J. Chem. 36, 1222-1240 (2018). 

    상세보기

활용도 Top5 논문

더보기

해당 논문의 주제분야에서 활용도가 높은 상위 5개 콘텐츠를 보여줍니다.
더보기 버튼을 클릭하시면 더 많은 관련자료를 살펴볼 수 있습니다.