Rhodium(III)-catalyzed oxidative olefination of N-(naphthalen-1-yl)amides

Synlett

Volumn 23, Issue 11, 2012, Pages 1649-1652

  Wang, Xiaowei ^a,b,c   Li, Xuting ^b   Xiao, Jian ^b   Jiang, Yi ^a   Li, Xingwei ^b  

^a CHENGDU INSTITUTE OF ORGANIC CHEMISTRY   (China)

^b DALIAN INSTITUTE OF CHEMICAL PHYSICS   (China)

^c UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

C H activation; oxidative olefination; rhodium

Indexed keywords

ACRYLIC ACID DERIVATIVE; AMIDE; BENZYL ACRYLATE; N (NAPHTHALEN 1 YL)ACETAMIDE; N (NAPHTHALEN 1 YL)AMIDE DERIVATIVE; N (NAPHTHALEN 1 YL)CARBOXAMIDE; RHODIUM; UNCLASSIFIED DRUG;

AMIDATION; AMINATION; ARTICLE; CATALYSIS; CHEMICAL ANALYSIS; CHEMICAL BOND; CHEMICAL STRUCTURE; CYCLIZATION; DEHALOGENATION; HYDROGEN BOND; NUCLEOPHILICITY; OLEFINATION; OXIDATION; OXIDATIVE COUPLING;

EID: 84862141663     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0031-1290428     Document Type: Article

References (32)

1. Jia C, Kitamura T, Fujiwara Y. Acc. Chem. Res: 2001; 34 633
2. Fujiwara Y, Moritani I, Matsuda M, Teranishi S. Tetrahedron Lett.: 1968; 9 633
3. Moritanl I, Fujiwara Y. Tetrahedron Lett.: 1967; 8 1119
4. Baran PS, Corey EJ. J. Am. Chem. Soc.: 2002; 124 7904
5. Beck EM, Hatley R, Gaunt MJ. Angew. Chem. Int. Ed.: 2008; 47 3004
6. Cushing TD, Sanz-Cervera JF, Williams RM. J. Am. Chem. Soc.: 1993; 115 9323
7. Garg NK, Caspi DD, Stoltz BM. J. Am. Chem. Soc.: 2004; 126 9552
8. Trost BM, Godleski SA, Genet JP. J. Am. Chem. Soc.: 1978; 100 3930
9. Wencel-Delord J, Dröge T, Liu F, Glorius F. Chem. Soc. Rev.: 2011; 40 4740
10. Yeung CS, Dong VM. Chem. Rev.: 2011; 111 1215
11. Colby DA, Bergman RG, Ellman JA. Chem. Rev.: 2009; 110 624
12. Satoh T, Miura M. Chem.-Eur. J.: 2010; 16 11212
13. Song G, Wang F, Li X. Chem. Soc. Rev.: 2012; 41 3651
14. Zhu C, Wang R, Falck JR. Chem.-Asian J.: 2012; in press; DOI: 10.1002/asia.201200035
15. Besset T, Kuhl N, Patureau FW, Glorius F. Chem.-Eur. J.: 2011; 17 7167
16. Patureau FW, Besset T, Glorius F. Angew. Chem. Int. Ed.: 2011; 50 1064
17. Patureau FW, Glorius F. J. Am. Chem. Soc.: 2010; 132 9982
18. Wencel-Delord J, Nimphius C, Patureau FW, Glorius F. Angew. Chem. Int. Ed.: 2012; 51 2247
19. Wencel-Delord J, Nimphius C, Patureau FW, Glorius F. Chem.-Asian J.: 2012; in press; DOI: 10.1002/asia.201101018
20. Rakshit S, Grohmann C, Besset T, Glorius F. J. Am. Chem. Soc.: 2011; 133 2350
21. Huestis MP, Chan L, Stuart DR, Fagnou K. Angew. Chem.: 2011; 123 1374
22. Rakshit S, Patureau FW, Glorius F. J. Am. Chem. Soc.: 2010; 132 9585
23. Stuart DR, Bertrand-Laperle MG, Burgess KM. N, Fagnou K. J. Am. Chem. Soc.: 2008; 130 16474
24. Du Y, Hyster TK, Rovis T. Chem. Commun.: 2011; 47 12074
25. Hyster TK, Rovis T. J. Am. Chem. Soc.: 2010; 132 10565
26. Hyster TK, Rovis T. Chem. Sci.: 2011; 2 1606
27. Song G, Chen D, Pan C.-L, Crabtree RH, Li X. J. Org. Chem.: 2010; 75 7487
28. Song G, Gong X, Li X. J. Org. Chem.: 2011; 76 7583
29. Su Y, Zhao M, Han K, Song G, Li X. Org. Lett.: 2010; 12 5462
30. Wang F, Song G, Du Z, Li X. J. Org. Chem.: 2011; 76 2926
31. Wang F, Song G, Li X. Org. Lett.: 2010; 12 5430
32. Wei X, Zhao M, Du Z, Li X. Org. Lett.: 2011; 13 4636