Subscribe to RSS
DOI: 10.1055/s-2007-984504
A Fluorinating Hypervalent Iodine(III) Reagent: 4-Iodotoluene Difluoride
Publication History
Publication Date:
25 June 2007 (online)
Introduction
There is a great interest of organic chemists in hypervalent iodine reagents because a wide range of reactions can be performed selectively under mild conditions and, in some cases, catalytically. [1] Fluorinated molecules are highly valuable due to the unique characteristics displayed by the fluorine atom. [2]
4-Iodotoluene difluoride (p-TolIF2, 1) is a hypervalent iodine reagent that promotes chemoselective fluorinations avoiding the use of fluorine gas, as well as the expensive xenon difluoride. Several N-fluoro compounds have been developed as stable and effective fluorinating reagents; their preparation, however, generally demands the use of fluorine gas. Compound 1 is usually preferred over its iodobenzene difluoride analogue because of easier preparation, purification, and handling.
-
1a
Stang PJ. J. Org. Chem. 2003, 68: 2997 -
1b
Wirth T. Angew. Chem. Int. Ed. 2005, 44: 3656 -
1c
Moriarty RM. J. Org. Chem. 2005, 70: 2893 -
1d
Silva LF. Molecules 2006, 11: 421 -
1e
Richardson RD.Wirth T. Angew. Chem. Int. Ed. 2006, 45: 4402 -
2a
Dolbier WR. J. Fluorine Chem. 2005, 126: 157 -
3a
Carpenter WJ. J. Org. Chem. 1966, 31: 2688 -
3b
Fuchigami T.Fujita T. J. Org. Chem. 1994, 59: 7190 -
3c
Sawaguchi M.Ayuba S.Hara S. Synthesis 2002, 1802 -
3d
Ye C.Twamley B.Shreeve JM. Org. Lett. 2005, 7: 3961 - 4
Arrica MA.Wirth T. Eur. J. Org. Chem. 2005, 395 - 5
Greaney MF.Motherwell WB. Tetrahedron Lett. 2000, 41: 4463 - 6
Greaney MF.Motherwell WB. Tetrahedron Lett. 2000, 41: 4467 - 7
Sato S.Yoshida M.Hara S. Synthesis 2005, 2602 - 8
Yoshida M.Fujikawa K.Sato S.Hara S. ARKIVOC 2003, (vi): 36 - 9
Hara S.Sekiguchi M.Ohmori A.Fukuhara T.Yoneda N. Chem. Commun. 1996, 1899 - 10
Hara S.Nakahigashi J.Ishi-i K.Fukuhara T.Yoneda N. Tetrahedron Lett. 1998, 39: 2589 - 11
Sawaguchi M.Hara S.Fukuhara T.Yoneda N. J. Fluorine Chem. 2000, 104: 277 - 12
Yoshida M.Kawakami K.Hara S. Synthesis 2004, 2821 -
13a
Yoshida M.Nagahara D.Fukuhara T.Yoneda N.Hara S. J. Chem. Soc., Perkin Trans. 1 2001, 1: 2283 -
13b
Yoshida M.Yoshikawa S.Fukuhara T.Yoneda N.Hara S. Tetrahedron 2001, 57: 7143 - 14
Yoshida M.Komata A.Hara S. J. Fluorine Chem. 2004, 125: 527 - 15
Panunzi B.Picardi A.Tingoli M. Synlett 2004, 2339 -
16a
Conte P.Panunzi B.Tingoli M. Tetrahedron Lett. 2006, 47: 273 -
16b
Conte P.Panunzi B.Tingoli M. Tetrahedron Lett. 2006, 47: 3325 - 17
Sawaguchi M.Hara S.Nakamura Y.Ayuba S.Fukuhara T.Yoneda N. Tetrahedron 2001, 57: 3315 - 18
Inagaki T.Nakamura Y.Sawaguchi M.Yoneda N.Ayuba S.Hara S. Tetrahedron Lett. 2003, 44: 4117