SynOpen, Table of Contents CC BY-NC-ND 4.0 · SynOpen 2021; 05(02): 134-137DOI: 10.1055/a-1480-8884 spotlight Rh(II)-Catalysed Condensations of N-Sulfonyl-1,2,3-triazoles with Aminals Nidal Saleh , Jérôme Lacour ∗ Recommend Article Abstract All articles of this category Abstract Key words Key wordsaminal - triazole - carbene - ylide - cascade Full Text References References 1a Meldal M, Tornøe CW. Chem. Rev. 2008; 108: 2952 1b Hein JE, Fokin VV. Chem. Soc. Rev. 2010; 39: 1302 1c Schulze B, Schubert US. Chem. Soc. Rev. 2014; 43: 2522 1d Tiwari VK, Mishra BB, Mishra KB, Mishra N, Singh AS, Chen X. Chem. Rev. 2016; 116: 3086 1e Haugland MM, Borsley S, Cairns-Gibson DF, Elmi A, Cockroft SL. ACS Nano 2019; 13: 4101 2a Kolb HC, Finn MG, Sharpless KB. Angew. Chem. Int. Ed. 2001; 40: 2004 2b Lewis WG, Green LG, Grynszpan F, Radić Z, Carlier PR, Taylor P, Finn MG, Sharpless KB. Angew. Chem. Int. Ed. 2002; 41: 1053 2c Amblard F, Cho JH, Schinazi RF. Chem. Rev. 2009; 109: 4207 2d Le Droumaguet C, Wang C, Wang Q. Chem. Soc. Rev. 2010; 39: 1233 2e Thirumurugan P, Matosiuk D, Jozwiak K. Chem. Rev. 2013; 113: 4905 3a Harmon RE, Stanley F, Gupta SK, Johnson J. J. Org. Chem. 1970; 35: 3444 3b Harmon RE, Earl RA, Gupta SK. J. Chem. Soc. D 1971; 296 3c Horneff T, Chuprakov S, Chernyak N, Gevorgyan V, Fokin VV. J. Am. Chem. Soc. 2008; 130: 14972 4a Chattopadhyay B, Gevorgyan V. Angew. Chem. Int. Ed. 2012; 51: 862 4b Gulevich AV, Gevorgyan V. Angew. Chem. Int. Ed. 2013; 52: 1371 4c Davies HM. L, Alford JS. Chem. Soc. Rev. 2014; 43: 5151 4d Anbarasan P, Yadagiri D, Rajasekar S. Synthesis 2014; 46: 3004 4e Wang Y, Lei X, Tang Y. Synlett 2015; 26: 2051 4f Jiang Y, Sun R, Tang X.-Y, Shi M. Chem. Eur. J. 2016; 22: 17910 5a Chuprakov S, Hwang FW, Gevorgyan V. Angew. Chem. Int. Ed. 2007; 46: 4757 5b Chuprakov S, Kwok SW, Zhang L, Lercher L, Fokin VV. J. Am. Chem. Soc. 2009; 131: 18034 5c Chuprakov S, Malik JA, Zibinsky M, Fokin VV. J. Am. Chem. Soc. 2011; 133: 10352 5d Zibinsky M, Fokin VV. Org. Lett. 2011; 13: 4870 5e Yadagiri D, Anbarasan P. Chem. Eur. J. 2013; 19: 15115 5f Schultz EE, Sarpong R. J. Am. Chem. Soc. 2013; 135: 4696 5g Miura T, Tanaka T, Matsumoto K, Murakami M. Chem. Eur. J. 2014; 20: 16078 5h Miura T, Nakamuro T, Liang C.-J, Murakami M. J. Am. Chem. Soc. 2014; 136: 15905 5i Yadagiri D, Anbarasan P. Org. Lett. 2014; 16: 2510 5j Medina F, Besnard C, Lacour J. Org. Lett. 2014; 16: 3232 5k Lindsay VN. G, Viart HM. F, Sarpong R. J. Am. Chem. Soc. 2015; 137: 8368 5l Kubiak RW, Mighion JD, Wilkerson-Hill SM, Alford JS, Yoshidomi T, Davies HM. L. Org. Lett. 2016; 18: 3118 5m Guarnieri-Ibáñez A, Medina F, Besnard C, Kidd SL, Spring DR, Lacour J. Chem. Sci. 2017; 8: 5713 5n Miura T, Zhao Q, Murakami M. Angew. Chem. Int. Ed. 2017; 56: 16645 5o Ma X, Xie X, Liu L, Xia R, Li T, Wang H. Chem. Commun. 2018; 54: 1595 5p Liu Z, Du Q, Zhai H, Li Y. Org. Lett. 2018; 20: 7514 5q Garlets ZJ, Davies HM. L. Org. Lett. 2018; 20: 2168 5r Jia R, Meng J, Leng J, Yu X, Deng WP. Chem. Asian J. 2018; 13: 2360 5s Yadagiri D, Chaitanya M, Reddy AC. S, Anbarasan P. Org. Lett. 2018; 20: 3762 5t Xu Z.-F, Shan L, Zhang W, Cen M, Li C.-Y. Org. Chem. Front. 2019; 6: 1391 5u De P B, Atta S, Pradhan S, Banerjee S, Shah TA, Punniyamurthy T. J. Org. Chem. 2020; 85: 4785 5v Reddy AC. S, Ramachandran K, Reddy PM, Anbarasan P. Chem. Commun. 2020; 56: 5649 5w Dequina HJ, Eshon J, Raskopf WT, Fernández I, Schomaker JM. Org. Lett. 2020; 22: 3637 5x Miura T, Nakamuro T, Ishihara Y, Nagata Y, Murakami M. Angew. Chem. Int. Ed. 2020; 59: 20475 6a Chuprakov S, Kwok SW, Fokin VV. J. Am. Chem. Soc. 2013; 135: 4652 6b Jeon HJ, Jung DJ, Kim JH, Kim Y, Bouffard J, Lee S.-g. J. Org. Chem. 2014; 79: 9865 6c Lee DJ, Han HS, Shin J, Yoo EJ. J. Am. Chem. Soc. 2014; 136: 11606 6d Lee DJ, Ko D, Yoo EJ. Angew. Chem. Int. Ed. 2015; 54: 13715 6e Lei X, Li L, He Y.-P, Tang Y. Org. Lett. 2015; 17: 5224 6f Xu H.-D, Jia Z.-H, Xu K, Zhou H, Shen M.-H. Org. Lett. 2015; 17: 66 6g Ryu T, Baek Y, Lee PH. J. Org. Chem. 2015; 80: 2376 6h Zhao Y.-Z, Yang H.-B, Tang X.-Y, Shi M. Chem. Eur. J. 2015; 21: 3562 6i Wang Y, Lei X, Tang Y. Chem. Commun. 2015; 51: 4507 6j Rostovskii NV, Ruvinskaya JO, Novikov MS, Khlebnikov AF, Smetanin IA, Agafonova AV. J. Org. Chem. 2017; 82: 256 7a Bosmani A, Guarnieri-Ibáñez A, Goudedranche S, Besnard C, Lacour J. Angew. Chem. Int. Ed. 2018; 57: 7151 7b Bosmani A, Guarnieri-Ibáñez A, Lacour J. Helv. Chim. Acta 2019; 102: e1900021 8 Saleh N, Bosmani A, Besnard C, Bürgi T, Jacquemin D, Lacour J. Org. Lett. 2020; 22: 7599 9 Ge J, Wu X, Bao X. Chem. Commun. 2019; 55: 6090 10 Guarnieri-Ibáñez A, de Aguirre A, Besnard C, Poblador-Bahamonde AI, Lacour J. Chem. Sci. 2021; 12: 1479 11 Haupert LJ, Poutsma JC, Wenthold PG. Acc. Chem. Res. 2009; 42: 1480
