Silver triflate catalyzed acetylation of alcohols, thiols, phenols, and amines

Synthesis

Volumn , Issue 10, 2011, Pages 1621-1625

  Das, Rima ^a   Chakraborty, Debashis ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY MADRAS   (India)

Author keywords

acetylation; alcohol; amine; phenol; silver triflate; thiol

Indexed keywords

ACETIC ANHYDRIDES; CATALYTIC QUANTITIES; HIGH YIELD; THIOL; TRIFLATES;

ACETYLATION; AMINES; ORGANIC POLYMERS; SILVER;

PHENOLS;

ALCOHOL DERIVATIVE; AMINE; PHENOL DERIVATIVE; THIOL DERIVATIVE;

ACETYLATION; ARTICLE; CATALYST; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONTROLLED STUDY; SYNTHESIS;

EID: 79955842459     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1259999     Document Type: Article

References (39)

1. Larock R C., Comprehensive Organic Transformations 2nd ed. VCH Weinheim 1989
2. Greene T W., Wuts P G. M., Protective Groups in Organic Synthesis 2nd ed. Wiley New York 1991
3. Greene T W., Wuts P G. M., Protective Groups in Organic Synthesis 3rd ed. Wiley New York 1999
4. Otera J, Esterification Wiley-VCH Weinheim 2003
5. Tomohumi S, Kousaburo O, Takeshi O, Synthesis 1999 1141
6. Scriven E F. V., Chem. Soc. Rev. 1983 12 129
7. Höfle G, Steglich W, Vorbrüggen H, Angew. Chem., Int. Ed. Engl. 1978 17 569
8. Iqbal J, Srivastava R R., J. Org. Chem. 1992 57 2001
9. Chandrasekhar S, Ramachandar T, Shyamsunder T, Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2004 43 813; and references cited therein
10. Baker R H., Bordwell F G., Org. Synth. 1955 3 141
11. Sarvari M H., Sharghi H, Tetrahedron 2005 61 10903
12. Tamaddon F, Amrollahi M A., Sharafat L, Tetrahedron Lett. 2005 46 7841
13. Chakraborti A K., Gulhane R, Tetrahedron Lett. 2003 44 3521
14. Chakraborti A K., Gulhane R, Synlett 2004 657
15. Bandgar B P., Kamble V T., Adavarte V S., Uppalla L S., Synlett 2002 735
16. Martin-Matute B, Edin M, Bogar K, Backvall J.-E, Angew. Chem. Int. Ed. 2004 43 6535
17. Bartoli G, Bosco M, Dalpozzo R, Marcantoni E, Massaccesi M, Rinaldi S, Sambri L, Synlett 2003 39
18. Ishii Y, Takeno M, Kawasaki Y, Muromachi A, Nishiyama Y, Sakaguchi S, J. Org. Chem. 1996 61 3088
19. Torregiani E, Seu G, Minassi A, Appendino G, Tetrahedron Lett. 2005 46 2193
20. Ghosh R, Swarupananda M, Chakraborty A, Tetrahedron Lett. 2005 46 147
21. Li A.-X, Li T.-S, Ding T.-H, Chem. Commun. 1997 1389
22. Kumareswaran R, Gupta A, Vankar Y D., Synth. Commun. 1997 27 277
23. Cope A C., Herrick E C., Org. Synth. 1963 4 304
24. Jin T.-S, Ma Y.-R, Zhang Z.-H, Li T.-S, Synth. Commun. 1998 28 3173
25. Orita A, Sakamoto K, Hamada Y, Mitsutome A, Otera J, Tetrahedron 1999 55 2899
26. Lee S G., Park J H., J. Mol. Catal. A: Chem. 2003 194 49
27. Berger B, Rabiller C G., Königsberger K, Faber K, Griengl H, Tetrahedron: Asymmetry 1991 1 541
28. Procopiou P A., Baugh S P. D., Flack S S., Inglis G G. A., J. Org. Chem. 1998 63 2342
29. Ishihara K, Kubota M, Kurihara H, Yamamoto H, J. Org. Chem. 1996 61 4560
30. Orita A, Tanahashi C, Kakuda A, Otera J, Angew. Chem. Int. Ed. 2000 39 2877
31. Orita A, Tanahashi C, Kakuda A, Otera J, J. Org. Chem. 2001 66 8926
32. Saravanan P, Singh V K., Tetrahedron Lett. 1999 40 2611
33. Chauhan K K., Frost C G., Love I, Waite D, Synlett 1999 1743
34. Ahmed N, VanLier J E., Tetrahedron Lett. 2006 47 5345
35. Tale R H., Adude R N., Tetrahedron Lett. 2006 47 7263
36. SrikanthReddy T, Narasimhulu M, Suryakiran N, ChinniMahesh K, Ashalatha K, Venkateswarlu Y, Tetrahedron Lett. 2006 47 6825
37. Wender P A., Handy S L., Wright D L., Chem. Ind. (London, U.K.) 1997 765
38. Chakraborty D, Gowda R R., Malik P, Tetrahedron Lett. 2009 50 6553
39. Das R, Chakraborty D, Synthesis 2011 277