Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2003(14): 2269-2272
DOI: 10.1055/s-2003-41443
DOI: 10.1055/s-2003-41443
PSP
© Georg Thieme Verlag Stuttgart · New York
Preparation of Chiral N-Vinyl Oxazolidinones by a Simple General Procedure
Further Information
Received
22 May 2003
Publication Date:
24 September 2003 (online)
Publication History
Publication Date:
24 September 2003 (online)
Abstract
A high yielding, general, and practical procedure for the N-vinylation of 2-oxazolidinones via TMSOTf-promoted dehydroalkoxylation of N,O-acetals is described.
Key words
oxazolidinone - N-vinylation - TMSOTf - N,O-acetal
-
1a
Montgomery J.Wieber GM.Hegedus LS. J. Am. Chem. Soc. 1990, 112: 6255 -
1b
Masters JJM.Hegedus LS.Tamariz J. J. Org. Chem. 1991, 56: 5666 -
1c
Laidig GJ.Hegedus LS. Synlett 1995, 527 -
2a
Miller M.Hegedus LS. J. Org. Chem. 1993, 58: 6779 -
2b
Bach T.Schröder J.Brandl T.Hecht J.Harms K. Tetrahedron 1998, 54: 4507 -
3a
Tamura O.Hashimoto M.Kobayashi Y.Katoh T.Nakatani K.Kamada M.Hayakawa I.Akiba T.Terashima S. Tetrahedron Lett. 1992, 33: 3487 -
3b
Akiba T.Hashimoto M.Kobayashi Y.Katoh T.Nakatani K.Kamada M.Hayakawa I.Terashima S. Tetrahedron 1994, 50: 3905 -
3c
Akiba T.Tamura O.Terashima S. Org. Synth. 1998, 75: 45 - 4
Walles WE,Tousignant WF, andHoutman T. inventors; US Patent 2891058 19590616. - 5
Shono T.Matsumura Y.Tsubata K.Sugihara Y.Yamane S.Kanazawa T.Aoki T. J. Am. Chem. Soc. 1982, 104: 6697 -
6a
Bach T.Brummerhop H. J. Prakt. Chem. 1999, 341: 312 -
6b
Bach T.Brummerhop H. J. Prakt. Chem. 1999, 341: 410 - 7
Gaulon C.Gizecki P.Dhal R.Dujardin G. Synlett 2002, 952 - 8
Gassman PG.Burns SJ.Pfister KB. J. Org Chem. 1993, 58: 1449 - 10
Dujardin G.Rossignol S.Brown E. Tetrahedron Lett. 1995, 36: 1653
References
Camphorsulfonic acid can be conveniently replaced by p-toluenesulfonic acid.
11In our hands the N-vinyl oxazolidinones obtained via Hg(II)-catalyzed exchange contained typically (even after distillation or SiO2 chromatography) 10-20% starting material.