Collect. Czech. Chem. Commun. 2009, 74, 995-1009
https://doi.org/10.1135/cccc2009020
Published online 2009-06-23 22:47:57

Preparation and structure of some sulfanylpropenylidene derivatives of Meldrum’s acid

Lynne A. Crawford and Hamish McNab*

School of Chemistry, The University of Edinburgh, West Mains Road, Edinburgh EH9 3JJ, UK

References

1. Blake A. J., McNab H., Monahan L. C.: J. Chem. Soc., Perkin Trans. 1 1989, 425. <https://doi.org/10.1039/p19890000425>
2. Blake A. J., McNab H., Monahan L. C.: J. Chem. Soc., Perkin Trans. 2 1991, 2003. <https://doi.org/10.1039/p29910002003>
3a. Hojo M., Masuda R., Okada E.: Chem. Lett. 1990, 2095. <https://doi.org/10.1246/cl.1990.2095>
3b. Hojo M., Masuda R., Okada E.: Synthesis 1991, 46. <https://doi.org/10.1055/s-1991-26377>
4. Meth-Cohn O., Suschitzky H.: Adv. Heterocycl. Chem. 1972, 14, 211. <https://doi.org/10.1016/S0065-2725(08)60954-X>
5a. Dyachenko E. V., Glukhareva T. V., Nikolaenko E. F., Tkachev A. V., Morzherin Y. Y.: Russ. Chem. Bull. 2004, 53, 1240. <https://doi.org/10.1023/B:RUCB.0000042280.71728.d0>
5b. Rabong C., Hametner C., Mereiter K., Kartsev V. G., Jordis U.: Heterocycles 2008, 75, 799. <https://doi.org/10.3987/COM-07-11260>
5c. Ryabukhin S. V., Plaskon A. S., Volochnyuk D. M., Pipko S. E., Tolmachev A. A.: Synth. Commun. 2008, 38, 3032. <https://doi.org/10.1080/00397910802044272>
6. Neuenschwander M., Neuenschwander A., Steinegger E., Engel P.: Helv. Chim. Acta 1979, 62, 609. <https://doi.org/10.1002/hlca.19790620228>
7. McNab H., Morel G., Stevenson E.: J. Chem. Res., Synop. 1997, 207. <https://doi.org/10.1039/a700453b>
8. Sauer J. C.: J. Am. Chem. Soc. 1957, 79, 5314. <https://doi.org/10.1021/ja01576a063>
9. Stevenson E.: Ph.D. Thesis. The University of Edinburgh, Edinburgh 1998.
10. Niewiadomski K. B., Suschitzky H.: J. Chem. Soc., Perkin Trans. 1 1975, 1679. <https://doi.org/10.1039/p19750001679>
11. Typical recipes are quoted in: McNab H., Stobie I.: J. Chem. Soc., Perkin Trans. 1 1982, 1845. <https://doi.org/10.1039/p19820001845>
12. Low J. N., Cobo J., Nogueras M., Sanchez A., Insuasty B., Torres H.: Acta Crystallogr., Sect. C: Cryst. Struct. Commun. 2002, 58, o39. <https://doi.org/10.1107/S0108270101018765>
13. Andreev G. N., Shults E. E., Volkov A. A., Shakirov M. M., Bagryanskaya I. Yu., Gatilov Yu. V., Tolstikov G. A.: Russ. J. Org. Chem. 2004, 40, 854. <https://doi.org/10.1023/B:RUJO.0000044549.81561.4f>
14. Novoa de Armas H., Blaton N. M., Peeters O. M., De Ranter C. J., Suárez M., Ochoa E., Verdecia Y., Salfrán E.: J. Chem. Crystallogr. 2000, 30, 189. <https://doi.org/10.1023/A:1009535215383>
15a. Reviews: Gaber A. M., McNab H.: Synthesis 2001, 2059. <https://doi.org/10.1055/s-2001-18057>
15b. McNab H.: Aldrichimica Acta 2004, 37, 19.
16. McNab H., Monahan L. C.: J. Chem. Soc., Perkin Trans. 1 1988, 863. <https://doi.org/10.1039/p19880000863>
17. Hunter G. A., McNab H.: J. Chem. Soc., Perkin Trans. 1 1995, 1209. <https://doi.org/10.1039/p19950001209>
18. Lin W., Sapountzis I., Knochel P.: Angew. Chem. Int. Ed. 2005, 44, 4258. <https://doi.org/10.1002/anie.200500443>
19. Creed T., Leardini R., McNab H., Nanni D., Nicolson I. S., Reed D.: J. Chem. Soc., Perkin Trans. 1 2001, 1079. <https://doi.org/10.1039/b009844m>
20. Pouchert J., Behnke J.: The Aldrich Library of 13C and 1H FT NMR Spectra. Aldrich Chemical Company Inc., Milwaukee 1993.