References
- Devon , T. K. and Scott , A. I. 1972 . “Handbook of Naturally Occurring Compounds” , Vol. 2 , 10 – 11 . 73 – 74 . 209 – 210 . 253 – 255 . 365 – 370 . New York : Academic Press .
- Thompson , J. E. , Walker , R. P. , Wratten , S. J. and Folkner , D. J. 1982 . Tetrahedron , 38 : 1865
- Dean , F. M. 1982 . “Advances in Heterocyclic Chemistry” , Edited by: Katritzky , A. R. Vol. 30 , 169 – 190 . New York : Academic Press .
- Tannis , S. P. 1982 . Tetreahedron Lett. , 23 : 3115
- Okabe , M. , Abe , A. and Tada , M. 1982 . J. Org. Chem. , 47 : 1775 M. Okabe and M. Tada, ibid, in press
- Schrauzer , G. N. 1968 . Inorg. Synth. , 11 : 62
- Burness , D. M. 1963 . Org. Synth. , Vol. 4 : 628 Coll. IR(CC14) 1067, 1030, and 874 cm−1; 1H-NMR(CC14) δ 2.00 (s, 3H), 6.11 (b. s, 1H), 7.09 (m, 1H), and 7.24 (t, 1H, J=1 Hz)
- Parker , K. A. and Johnson , W. S. 1969 . Tetrahedron Lett. , : 1329 IR(CC14) 1212, 1077, 1025, and 876 cm−1; 1H-NMR (CC14) δ 4.38(s, 2H), 6.37(b. s, 1H), 7.33(t, 1H, J=1 Hz), and 7.41(m, 1H)
- IR(KBr) 1435, 1103, 871, and 690 cm−1; 1H-NMR (CF3COOH) δ(TSP standard) 4.37(d, 2H, J=14 Hz), 5.87(b. s, 1H), 7.04(dif.d, 1H, J=4 Hz), and 7.38–7.90(m, 15H)
- Matsumoto , T. and Usui , S. 1978 . Chem. Lett. , : 105 S. Araki and Y. Butsugan, ibid, 1982, 177
- Cimino , G. , DeStefano , S. , Minale , L. and Trivellone , E. 1972 . Tetrahedron , 28 : 4761 IR (CC14) 1049, 1029, and 877 cm−1; 1H-NMR(CC14) δ 0.88 (d, 9H, J=6 Hz), 1.05–1.25 (m, 12H), 2.37(t, 2H, J=7 Hz), 6.14(b. s, 1H), 7.11(m, 1H), and 7.23(t, 1H, J=1 Hz)
- (3-Chloromethyl) furan can be prepared from commercially available (3-hydroxymethyl) furan (Aldrich: 25g/$ 64.15)