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Synlett 2005(16): 2510-2512
DOI: 10.1055/s-2005-872693
DOI: 10.1055/s-2005-872693
LETTER
© Georg Thieme Verlag Stuttgart · New York
Photochemical Desulfonylation of N-Tosyl Amides by 2-Phenyl-N,N′-Dimethylbenzimidazoline (PDMBI)
Weitere Informationen
Received
28 July 2005
Publikationsdatum:
21. September 2005 (online)
Publikationsverlauf
Publikationsdatum:
21. September 2005 (online)

Abstract
Photoinduced electron transfer reaction between N-tosyl amides and 2-phenyl-N,N′-dimethylbenzimidazoline (PDMBI) provides an efficient approach for the desulfonylation of N-tosyl amides.
Key words
N-tosyl amides - deprotection - photoinduced electron transfer - 2-phenyl-N,N′-dimethylbenzimidazoline
-
1a
Greene TW.Wuts PGM. Protective Groups in Organic Synthesis 3rd ed.: Wiley-Interscience; New York: 1999. -
1b
Kocienski PJ. Protecting Groups Thieme; New York: 1994. -
2a
Nagashima H.Ozaki N.Washiyama M.Itoh K. Tetrahedron Lett. 1985, 26: 657 -
2b
Alonso E.Ramón DJ.Yus M. Tetrahedron 1997, 53: 14355 - 3
Roemmele RC.Rapaport H. J. Org. Chem. 1988, 53: 2367 - 4
Knowles H.Parsons AF.Pettifer RM. Synlett 1997, 271 - 5
Nyasse B.Grehn L.Ragnarsson U. Chem. Commun. 1997, 1017 - 6
Yasuhara A.Sakamoto T. Tetrahedron Lett. 1998, 39: 595 - 7
Sabitha G.Reddy BVS.Abraham S.Yadav JS. Tetrahedron Lett. 1999, 40: 1569 -
8a
Parsons AF.Pettifer RM. Tetrahedron Lett. 1996, 37: 1667 -
8b
Knowles HS.Parsons AF.Pettifer RM.Rickling S. Tetrahedron 2000, 56: 979 -
9a
Pete JP.Portella C. J. Chem. Res., Miniprint 1979, 209 -
9b
Li C.Fuchs PL. Tetrahedron Lett. 1993, 34: 1855 -
9c
Hamada T.Nishida A.Yonemitsu O. J. Am. Chem. Soc. 1986, 108: 140 -
9d
Art JF.Kestemont JP.Soumillion JP. Tetrahedron Lett. 1991, 32: 1425 -
10a
Chikashita H.Ide H.Itoh K. J. Org. Chem. 1986, 51: 5400 -
10b
Chikashita H.Itoh K. Bull. Chem. Soc. Jpn. 1986, 59: 1747 -
10c
Chen J.Tanner DD. J. Org. Chem. 1988, 53: 3897 -
10d
Tanner DD.Chen JJ. J. Org. Chem. 1989, 54: 3842 -
10e
Tanner DD.Chen JJ.Chen L.Luelo C. J. Am. Chem. Soc. 1991, 113: 8074 -
10f
Tanner DD.Chen JJ. J. Org. Chem. 1992, 57: 662 -
10g
Lee I.-SH.Jeoung EH.Kreevoy MM. J. Am. Chem. Soc. 2001, 123: 7492 -
10h
Hasegawa E.Yoneoka A.Suzuki K.Kato T.Kitazume T.Yanagi K. Tetrahedron 1999, 55: 12957 -
10i
Hasegawa E.Chiba N.Nakajima A.Suzuki K.Yoneoka A.Iwaya K. Synthesis 2001, 1248 -
10j
Hasegawa E.Takizawa S.Iwaya K.Kurokawa M.Chiba N.Yamamichi K. Chem. Commun. 2002, 1966 -
10k
Hasegawa E.Chiba N.Takahashi T.Takizawa S.Kitayama T.Suzuki T. Chem. Lett. 2004, 33: 18 - 11
Jin MZ.Yang L.Wu LM.Liu YC.Liu Z.-L. Chin. Chem. Lett. 2001, 12: 307 - 12
Casadei MA.Gessner A.Inesi A.Jugelt W.Moracci FM. J. Chem. Soc., Perkin Trans. 1 1992, 2001 - 14
Mella M.Fagnoni M.Freccero M.Fasani E.Albini A. Chem. Soc. Rev. 1998, 27: 81 -
15a
Maslak P.Narvaez JN. Angew. Chem., Int. Ed. Engl. 1990, 29: 283 -
15b
Maslak P.Kula J.Chateauneuf JE. J. Am. Chem. Soc. 1991, 113: 2304
References
For example 2b: MS (EI): m/z (rel. int.) = 191 (13), 149 (32), 106 (48), 91 (100), 77 (14). 1Η ΝMR (300 MHz, CDCl3): δ = 7.26 m (5 H), 6.42 (br s, 1 H), 4.35 (d, J = 5.7 Hz, 2 H), 2.17 (t, J = 7.5 Hz, 2 H), 1.59 (quin, J = 7.5 Hz, 2 H), 1.28 (sext, J = 7.5 Hz, 2 H), 0.88 (t, J = 7.5 Hz, 3 H). 13C NMR (75 MHz): δ = 173.2, 138.4, 128.4, 127.5, 127.2, 43.2, 36.2, 27.7, 22.3, 13.6.