Collect. Czech. Chem. Commun.
2002, 67, 235-244
https://doi.org/10.1135/cccc20020235
Direct Preparation of N-(Alk-1-en-1-yl)carbamates from Cyclic Ketones and Unsubstituted Carbamates
Philippe Dupau, Anne-Emmanuelle Hay, Célia Alameda Angulo, Pierre H. Dixneuf and Christian Bruneau*
Institut de Chimie de Rennes, UMR 6509: CNRS-Université de Rennes, Organométalliques et Catalyse, Campus de Beaulieu, 35042 Rennes Cedex, France
References
1. J. Am. Chem. Soc. 1982, 104, 6697.
< T., Matsumura Y., Tsubata K., Sugihara Y., Yamane S.-I., Kanazawa T., Aoki T.: https://doi.org/10.1021/ja00388a037>
2. Tetrahedron Lett. 1998, 39, 3413.
< C. H., Carroll P. J., Correia C. R. D.: https://doi.org/10.1016/S0040-4039(98)00536-X>
3a. J. Chem Soc., Perkin Trans. 1 1996, 1833.
< B., Rudyk H., Toupet L., Danion-Bougot R., Danion D.: https://doi.org/10.1039/p19960001833>
3b. Synthesis 1994, 1171.
< B., Danion-Bougot R., Danion D.: https://doi.org/10.1055/s-1994-25666>
4a. Tetrahedron Lett. 1999, 40, 7735.
< P. C. M. L., Correia C. R. D.: https://doi.org/10.1016/S0040-4039(99)01638-X>
4b. Tetrahedron Lett. 1997, 38, 1869.
< M. J. S., Miranda P. C. M. L., Correia C. R. D.: https://doi.org/10.1016/S0040-4039(97)00238-4>
5. J. Org. Chem. 1998, 63, 684.
< A. B., Hegedus L. S.: https://doi.org/10.1021/jo971665v>
6. Tetrahedron Lett. 1999, 40, 2083.
< D. F., Severino E. A., Correia C. R. D.: https://doi.org/10.1016/S0040-4039(99)00151-3>
7a. J. Organomet. Chem. 1975, 90, 363.
H. B., Langlois N., Dang T. P.:
7b. J. Org. Chem. 1987, 52, 5143.
< D. G., Larsen R. D., Mathre D. J., Shukis W. F., Wood A. W., Colleluori J. R.: https://doi.org/10.1021/jo00232a016>
7c. Tetrahedron: Asymmetry 1999, 10, 3863.
< X., Yeung C.-H., Chan A. S. C., Lee D.-S., Yang T.-K.: https://doi.org/10.1016/S0957-4166(99)00424-3>
8. Tetrahedron Lett. 1999, 40, 6685.
< M. J., Johnson N. B., Lee J. R.: https://doi.org/10.1016/S0040-4039(99)01376-3>
9. J. Chem Soc., Perkin Trans. 1 1998, 1403.
< A., Deniau E., Lebrun P., Grandclaudon P., Carpentier J.-F.: https://doi.org/10.1039/a709053f>
10. J. Org. Chem. 1998, 63, 1806.
< P., Thominot P., Bruneau C., Dixneuf P. H.: https://doi.org/10.1021/jo971733d>
11a. Chem. Rev. (Washington, D. C.) 1996, 96, 835.
< D. J., Prakash I., Schaad D. R.: https://doi.org/10.1021/cr9500038>
11b. Aldrichim. 1982, 15, 23.
D. A.:
12. Tetrahedron: Asymmetry 1999, 10, 3467.
< P., Bruneau C., Dixneuf P. H.: https://doi.org/10.1016/S0957-4166(99)00375-4>
13a. J. Org. Chem. 1981, 46, 4791.
< G. A., Neuenschwander K.: https://doi.org/10.1021/jo00336a036>
13b. Chem. Lett. 1977, 693.
< Y., Ogawa K., Takeuchi Y., Tomoda S.: https://doi.org/10.1246/cl.1977.693>
14a. J. Org. Chem. 1996, 61, 4180.
< R. K., Sharma R. R.: https://doi.org/10.1021/jo960153y>
14b. J. Org. Chem. 1999, 64, 6646.
< D. F., Miranda P. C. M. L., Correia C. R. D.: https://doi.org/10.1021/jo9903297>
15. Tetrahedron 1995, 51, 11075.
< P., Barth L.: https://doi.org/10.1016/0040-4020(95)00681-W>
16a. Tetrahedron Lett. 1985, 26, 85.
< C., Yonezawa Y., Watanabe E.: https://doi.org/10.1016/S0040-4039(00)98474-0>
16b. Chem. Lett. 1981, 1635.
< C., Yonezawa Y., Yoshimura J.: https://doi.org/10.1246/cl.1981.1635>
16c. Synthesis 1996, 1459.
< P., Conesa C., Desamparados V. M.: https://doi.org/10.1055/s-1996-4410>
17a. Bull. Chem. Soc. Jpn. 1980, 53, 2905.
< Y., Shin C., Ono Y., Yoshimura J.: https://doi.org/10.1246/bcsj.53.2905>
17b. Heterocycles 1989, 28, 589.
< U., Pavone V.: https://doi.org/10.3987/COM-88-S61>
18. Synlett 1999, 1832.
< P., Le Gendre P., Bruneau C., Dixneuf P. H.: https://doi.org/10.1055/s-1999-2937>
18b. Adv. Synth. Catal. 2001, 343, 331.
< P., Bruneau C., Dixneuf P. H.: https://doi.org/10.1002/1615-4169(20010430)343:4<331::AID-ADSC331>3.0.CO;2-A>
19. J. Org. Chem. 1995, 60, 4324.
< D. M., Abramson L., Cai D., Desmond R., Dolling U.-H., Frey L., Karady S., Shi Y.-J., Verhoeren T. R.: https://doi.org/10.1021/jo00119a008>