Subscribe to RSS
DOI: 10.1055/s-2006-958925
Intermolecular Mn(OAc)3-Mediated Oxidative Free-Radical Reaction of Dimethyl Malonate or Ethyl Cyanoacetate with Allenes: An Efficient Synthesis of Furan-2(5H)-ones or Dimethyl 2-(2-Oxoethylidene)malonates
Publication History
Publication Date:
12 December 2006 (online)
Abstract
Manganese(III)-mediated free-radical reaction of allenes with dimethyl malonate or ethyl cyanoacetate in acetic acid produces furan-2-(5H)-one derivatives (but-2-en-4-olides) or dimethyl 2-(2-oxoethylidene)malonates in moderate yields. The possible reaction mechanism is also discussed.
Key words
allene - radical reaction - manganese(III)
- For reviews of manganese(III)-mediated reactions:
-
1a
Curran DP. Synthesis 1988, 417 -
1b
Curran DP. Synthesis 1988, 489 -
1c
Jasperse CP.Curran DP. Chem. Rev. 1991, 91: 1237 -
1d
Melikyan GG. Synthesis 1993, 833 -
1e
Snider BB. Chem. Rev. 1996, 96: 339 -
1f
Melikyan GG. Org. React. 1997, 49: 427 -
1g
Radicals in Organic Synthesis
Vol. 1:
Renaud P.Sibi MP. Wiley-VCH; Weinheim: 2001. p.198-218 - For some of the most recent examples, see:
-
2a
Snider BB.Kiselgof JY.Foxman BM. J. Org. Chem. 1998, 63: 7945 -
2b
Zoretic PA.Fang H. J. Org. Chem. 1998, 63: 7213 -
2c
Cossy J.Bouzide A. Tetrahedron 1999, 55: 6483 -
2d
Yang D.Ye XY.Xu M. J. Org. Chem. 2000, 65: 2208 -
2e
Jiang MC.Chuang CP. J. Org. Chem. 2000, 65: 5409 -
2f
Yang D.Ye XY.Xu M.Pang KW.Cheung KK. J. Am. Chem. Soc. 2000, 122: 1658 -
2g
Yang D.Xu M.Bian MY. Org. Lett. 2001, 3: 111 -
2h
Snider BB.Smith RB. Tetrahedron 2002, 58: 25 -
3a
Landor SR. In The Chemistry of the Allene Vol. 1-3: Academic Press; London: 1982. -
3b
Schuter HF.Coppolar GM. Allenes in Organic Synthesis Wiley; New York: 1984. -
3c
The Chemistry of Ketenes, Allenes and Related Compounds
Patai S. Wiley; Chichester: 1980. Parts 1 and 2. - For reviews of radical reaction of allenes, see:
-
4a
Griesbaum K. Angew. Chem., Int. Ed. Engl. 1966, 5: 933 -
4b
Pasto DJ. Tetrahedron 1984, 40: 2805 -
5a
Marco-Contelles J.Balme G.Bouyssi D.Destabel C.Henriet-Bernard CD.Grimaldi J.Hatem JM. J. Org. Chem. 1997, 62: 1202 -
5b
Hölemann A.Reissig H.-U. Org. Lett. 2003, 5: 1463 -
5c
Hölemann A.Reissig H.-U. Chem. Eur. J. 2004, 10: 5493 -
5d
Molander GA.Cormier EP. J. Org. Chem. 2005, 70: 2622 - 6 A literature survey shows that only one example of manganese(III)-mediated intramolecular reaction of the allenic diester has been reported, see:
Okuro K.Alper H. J. Org. Chem. 1996, 61: 5312 - 7
Zhou H.Huang X.Chen W. J. Org. Chem. 2004, 69: 5471 - Generally speaking, regioselectivities of free-radical additions to allenes range from complete terminal attack to exclusive central addition depending on the reaction conditions, see:
-
9a
Kuivila HG.Rahman W.Fish RH. J. Am. Chem. Soc. 1965, 87: 2835 -
9b
Pasto DA.L’Hermine G. J. Org. Chem. 1990, 55: 685 - 10
Linker T. J. Organomet. Chem. 2002, 661: 159 ; and references cited therein - Other examples of manganese(III)-mediated lactonizations of diesters, see:
-
11a
Citterio A.Marion A.Nicolini M. Tetrahedron Lett. 1993, 34: 7981 -
11b
Citterio A.Sebastiano R.Marion A. J. Org. Chem. 1991, 56: 5328 -
11c
Linker T.Kersten B.Linker U.Peters K.Peters EM.Schnering HG. Synlett 1996, 468 -
11d
Crocker PJ.Miller MJ. J. Org. Chem. 1995, 60: 6176 -
11e
Dombroski MA.Kates SA.Snider BB. J. Am. Chem. Soc. 1990, 112: 2795 - 12
March J. Advanced Organic Chemistry, Reaction, Mechanism, and Structure 4th ed: John Wiley & Sons; New York: 1992. p.pp 1123 - For some recent reviews and examples, see:
-
13a
Negishi E.Kotora M. Tetrahedron 1997, 53: 6707 -
13b
Takahashi S.Maeda K.Hirota S.Nakakta T. Org. Lett. 1999, 1: 2025 -
13c
Marshall JA.Piettre A.Paige MA.Valeriote F. J. Org. Chem. 2003, 68: 1780 -
13d
Trost BM.Toste FD. J. Am. Chem. Soc. 2003, 125: 3090 -
13e
Yoneda E.Kaneko T.Zhang S.Onitsuka K.Takahashi S. Org. Lett. 2000, 2: 441 -
13f
Linclau B.Boydell AJ.Clarke PJ.Horan R.Jaequet C. J. Org. Chem. 2003, 68: 1821 - 14
Iesce MR.Cermola F.Piazza A.Scarpati R.Graziano ML. Synthesis 1995, 439
References
Crystal data for compound 5a: C15H16O5, M = 276.28, triclinic, space group P-1, Mo KR, final R indices [I > 2 σ(I)], R 1 = 0.0562, wR 2 = 0.1254, a = 5.6333 (10), b = 8.1532 (14), c = 15.953 (3) Å, α = 96.899 (4)°, β = 91.399 (3)°, γ = 92.189 (4)°, V = 726.5 (2) Å3, T = 293 (2) K, Z = 2, reflections collected/unique: 4300/3079 (R int = 0.0933), no observation [I > 2 σ(I)] 3079, parameters 194.