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Synthesis 2004(16): 2637-2640
DOI: 10.1055/s-2004-831231
DOI: 10.1055/s-2004-831231
PAPER
© Georg Thieme Verlag Stuttgart · New York
A Tandem Nucleophilic Addition, Defluorination and Destannylation. Stereospecific Synthesis of Trifluoromethylated Alkyl and Aryl Vinyl Ethers
Weitere Informationen
Received
7 June 2004
Publikationsdatum:
22. September 2004 (online)
Publikationsverlauf
Publikationsdatum:
22. September 2004 (online)
Abstract
A novel tandem reaction, including nucleophilic addition, defluorination and destannylation reactions, has been found and its application to the stereospecific synthesis of trifluorometh-ylated alkyl- and aryl vinyl ethers with exclusive formation of E-isomers in 73-96% yields is reported. An AdN -E mechanism for the tandem reaction leading to alkyl- and aryl vinyl ethers is proposed.
Key words
trifluoromethylated alkyl- and aryl vinyl ethers - nucleophilic addition - defluorination - destannylation
-
1a
Giessert AJ.Snyder L.Markham J.Diver ST. Org. Lett. 2003, 5: 1793 -
1b
Kobayashi S.Matsubara R.Nakamura Y.Kitagawa H.Sugiura M. J. Am. Chem. Soc. 2003, 125: 2507 -
1c
Amantini D.Fringuelli F.Pizzo F. J. Org. Chem. 2002, 67: 7238 -
1d
Pham W.Weissleder R.Tung CH. Tetrahedron Lett. 2002, 43: 19 -
1e
Xu L.Chen W.Ross J.Xiao J. Org. Lett. 2001, 3: 295 -
1f
Uchiyama M.Satoh S.Ohta A. Tetrahedron Lett. 2001, 42: 1559 -
1g
Katritzky AR.Fang YF.Silina A. J. Org. Chem. 1999, 64: 7622 -
2a
Nakamura Y.Matsubara R.Kiyohara H.Kabayashi S. Org. Lett. 2003, 5: 2481 -
2b
Savinov SN.Austin DJ. Org. Lett. 2002, 4: 1415 -
2c
Kulkarni MG.Rasne RM.Davawala SI.Doke AK. Tetrahedron Lett. 2002, 43: 2297 -
2d
Harrowven DC.Tyte MJ. Tetrahedron Lett. 2002, 43: 5971 -
2e
Jensen KB.Roberson M.Jorgensen KA. J. Org. Chem. 2000, 65: 9080 -
2f
Zhuang W.Thorhauge J.Jorgensen KA. Chem. Commun. 2000, 459 - 3
Yu W.Jin Z. J. Am. Chem. Soc. 2000, 122: 9840 ; and references cited therein - 4
Friesen RW. J. Chem. Soc., Perkin Trans. 1 2001, 1969 ; and references cited therein -
5a
Reppe W. Liebigs Ann. Chem. 1956, 601: 81 -
5b
Trofimov BA.Vasil’tsov AM.Schmidt EY.Zaitsev AB.Mikhaleva AI.Afonin AV. Synthesis 2000, 1521 -
6a
Surprenant S.Chan WY.Berthelette C. Org. Lett. 2003, 5: 4851 -
6b
Okimoto Y.Sakaguchi S.Ishii Y. J. Am. Chem. Soc. 2002, 124: 1590 ; and references cited therein -
6c
Bosch M.Schlaf M. J. Org. Chem. 2003, 68: 5225 -
6d
Blouin M.Frenette R. J. Org. Chem. 2001, 66: 9043 -
6e
Chakravarty M.Srinivas B.Muthiah C.Swamy KCK. Synthesis 2003, 2368 -
6f
Roeschlaub CA.Sammes PG. J. Chem. Soc., Perkin Trans. 1 2000, 2243 -
7a
Begue J.-P.Bonnet-Delpon D.Mesureur D.Nee G.Wu SW. J. Org. Chem. 1992, 57: 3807 -
7b
Hong F.Hu C.-M. Chem. Commun. 1996, 57 -
7c
Shi G.-Q.Huang X.-H.Hong F. J. Chem. Soc., Perkin Trans. 1 1996, 763 -
7d
Shi G.-Q.Huang X.-H.Hong F. J. Org. Chem. 1996, 61: 3200 -
7e
Purrington ST.Thomas HN. J. Fluorine Chem. 1998, 90: 47 -
7f
Zhu SZ.Jin GF.Peng WM.Huang QC. Tetrahedron 2003, 59: 2899 ; and references cited therein -
8a
Shen Y.Wang G. Org. Lett. 2002, 4: 2083 -
8b
Shen Y.Wang G. Synthesis 2002, 209 - 9
McCarthy JR.Matthews DP.Stemerick DM.Huber EW.Bey P.Lippert BJ.Snyder RD.Sunkara PS. J. Am. Chem. Soc. 1991, 113: 7439 - 10
Cullen WR.Waldman MC. Can. J. Chem. 1969, 47: 3093