Abstract
Sundry dipropargyloxy disulfides have been successfully prepared and their rearrangement paths and products have been found to be dependent upon their substitution pattern. Inter alia compounds of two heretofore unknown structure types - 10 and 11 on the one hand and 14 and 15 on the other - have been obtained and characterized.
Original language | English |
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Pages (from-to) | 1333-1337 |
Number of pages | 5 |
Journal | Phosphorus, Sulfur and Silicon and the Related Elements |
Volume | 180 |
Issue number | 5-6 |
DOIs | |
State | Published - May 2005 |
Bibliographical note
Funding Information:Received July 9, 2004; accepted October 5, 2004. This research was supported by the Israel Science Foundation (Grant No. 280/01-1). Address correspondence to Samuel Braverman, Department of Chemistry, Bar-Ilan University, Ramat-Gan 52900, Israel. E-mail: [email protected]
Funding
Received July 9, 2004; accepted October 5, 2004. This research was supported by the Israel Science Foundation (Grant No. 280/01-1). Address correspondence to Samuel Braverman, Department of Chemistry, Bar-Ilan University, Ramat-Gan 52900, Israel. E-mail: [email protected]
Funders | Funder number |
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Israel Science Foundation | 280/01-1 |
Keywords
- Cycloaddition
- Propargylic dialkoxy disulfides
- Sigmatropic rearrangement
- Sulfine
- Synthesis
- Thioaldehyde