SYNTHESES VIA VINYL SULFONES .75. TRIFLONE CHEMISTRY .10. SCOPE AND LIMITATIONS OF FUNCTIONALIZED ACETYLENIC TRIFLONES IN THE DIRECT ALKYNYLATION OF C-H BONDS

Citation
J. Xiang et al., SYNTHESES VIA VINYL SULFONES .75. TRIFLONE CHEMISTRY .10. SCOPE AND LIMITATIONS OF FUNCTIONALIZED ACETYLENIC TRIFLONES IN THE DIRECT ALKYNYLATION OF C-H BONDS, Tetrahedron letters, 38(38), 1997, pp. 6635-6638
Citations number
6
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
38
Issue
38
Year of publication
1997
Pages
6635 - 6638
Database
ISI
SICI code
0040-4039(1997)38:38<6635:SVVS.T>2.0.ZU;2-B
Abstract
Reactions of TIPS-substituted acetylenic triflones extends the versati lity of the trifluoromethyl radical mediated C-H alkynylation reaction , Alkynes bearing acetylenic or propargylic oxygen functionality canno t be prepared, but silyl ethers or chlorides in remote positions may b e carried through the reaction. Crown ethers are successfully monofunc tionalized and distal bis-acetylenes may be employed in the title reac tion. (C) 1997 Elsevier Science Ltd.