References
- Levi, L. E. Chem. News. 1890, 62, 216.
- (a) Parham, W. E.; Wynberg, H.; Ramp, F. L. J. Am. Chem. Soc. 1953, 75, 2065–2069. DOI: 10.1021/ja01105a013. (b) Parham, W. E.; Heberling, J.; Wynberg, H. J. Am. Chem. Soc. 1955, 77, 1169–1174. DOI: 10.1021/ja01105a013.
- (a) Schroth, W.; Peschel, J. Z Chem. 2010, 4, 271–271. DOI: 10.1002/zfch.19640040706. (b) Bottini, A. T.; Böttner, E. F. J. Org. Chem. 1966, 31, 586–587. DOI: 10.1021/jo01340a502. (c) Rubinstein, H.; Wuerthele, M. J. Org. Chem. 1969, 34, 2762–2763. DOI: 10.1021/jo01261a061. (d) Asinger, F.; Saus, A.; Offermanns, H.; Scherberich, P. Justus Liebigs Ann. Chem. 1971, 753, 151–168. DOI: 10.1002/jlac.19717530114. (e) Yoshino, H.; Kawazoe, Y.; Taguchi, T. Synthesis. 1974, 1974, 713–715. DOI: 10.1055/s-1974-23411.
- Caputo, R.; Ferreri, C.; Palumbo, G.; Capozzi, G. Tetrahedron. 1986, 42, 2369–2376. DOI: 10.1016/S0040-4020(01)90619-2.
- Afonso, C. A. M.; Barros, M. T.; Godinho, L. S.; Maycock, C. D. Synthesis. 1991, 1991, 575–580. DOI: 10.1055/s-1991-26520.
- Russell, G. A.; Law, W. C.; Zaleta, M. J. Am. Chem. Soc. 1985, 107, 4175–4182. DOI: 10.1021/ja00300a016.
- Caputo, R.; Ferreri, C.; Palumbo, G. Synthesis. 1991, 1991, 223–224. DOI: 10.1055/s-1991-26427.
- Nakayama, J.; Nakamura, Y.; Hoshino, M. Heterocycles. 1985, 23, 1119–1122. DOI: 10.3987/R-1985-01-0215.
- (a) Caputo, R.; Ferreri, C.; Longobardo, L.; Mastroianni, D.; Palumbo, G.; Pedatell, S. Synth. Commun. 1994, 24, 1223–1229. DOI: 10.1080/00397919408011721. (b) Caputo, R.; Palumbo, G.; Pedatella, S. S. Tetrahedron. 1994, 50, 7265–7268. DOI: 10.1016/S0040-4020(01)85249-2.
- Witczak, Z. J.; Bielski, R. Domino Intramolecular Rearrangement Reactions as Advanced Synthetic Methods in Glycoscience, 1st ed. J. Wiley & Sons Inc., 2016, ISBN: 978-1-119-04439-0; Chart 5. D’Alonzo, D.; Palumbo, G.; Guaragna, A. Multistep Transformations of Bis-Thioenol Ether-containing Chiral Building Blocks: New Avenues in Glycochemistry; pp 97–113.
- Buszta, N.; Depa, W. J.; Bajek, A.; Groszek, G. Chem. Pap. 2019, 73, 2885–2888. DOI: 10.1007/s11696-019-00837-3.
- (a) Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Chemistry, 3rd ed. New York: J. Wiley & Sons Inc., 1999. (b) Barrett, A. G. M.; Rys, D. J. J. Chem. Soc. Perkin Trans. 1995, 1, 1009–1017. (c) Fieser, L. F. J. Am. Chem. Soc. 1954, 76, 1945–1947. DOI: 10.1021/ja01636a063.
- CCDC 1998115-1998116 records contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from the joint CCDC’s and FIZ Karlsruhe’s service to view and retrieve structures via https://www.ccdc.cam.ac.uk/structures/. See also SI.
- Unpublished result. During dithioacetalization of (R)-2-((t-butyldimethylsilyl)oxy)propanal or (S)-2-((tributylsilyl)oxy)propanal deprotection of hydroxyl group took plase.
- Wood, W. W. Trends in the Chemistry of 1,3-Dithioacetals. In Organosulfur Chemistry, Synthetic Aspects, Chapter 4; Page, P., Ed.; Academic Press: London, 1995; pp 133–224.
- Sromek, A. W.; Gevorgyan, V. 1. 2-Sulfur Migrations. Vol. 274. In Sulfur-Mediated Rearrangements, Topics in Current Chemistry, 1st ed.; Springer: Berlin, Heidelberg, 2007; pp 110–114.