New structures from multiple rearrangements of propargylic dialkoxy disulfides

Samuel Braverman, Tatiana Pechenick, Hugo E. Gottlieb, Milon Sprecher

Research output: Contribution to journalArticlepeer-review

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 languageEnglish
Pages (from-to)1333-1337
Number of pages5
JournalPhosphorus, Sulfur and Silicon and the Related Elements
Volume180
Issue number5-6
DOIs
StatePublished - 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]

FundersFunder number
Israel Science Foundation280/01-1

    Keywords

    • Cycloaddition
    • Propargylic dialkoxy disulfides
    • Sigmatropic rearrangement
    • Sulfine
    • Synthesis
    • Thioaldehyde

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