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Synthesis 2003(2): 0288-0294
DOI: 10.1055/s-2003-36825
DOI: 10.1055/s-2003-36825
PAPER
© Georg Thieme Verlag Stuttgart · New York
Synthesis of Polyfunctional Organosulfur Compounds Mediated by Azetidinium Salts
Further Information
Received
5 August 2002
Publication Date:
22 January 2003 (online)
Publication History
Publication Date:
22 January 2003 (online)

Abstract
Ring-opening of N,N-dialkyl-3-hydroxyazetidinium chlorides 1a-d with sulfur nucleophiles leads to C-S bond formation furnishing polyfunctional sulfides, sulfonates and thiosulfonates.
Key words
alkylation - heterocycles - nucleophiles - ring opening - sulfonates
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References
For example: 4b = MOPSO sodium salt: Fluka 69941, Sigma M5914.
18The higher than commonly acceptable differences between calculated and found data of some elemental analyses for compounds 2 and 4 can arise from contamination with NaCl which is hard to remove by crystallization. The purified salt 2d (column chromatography) may contain trace amounts of the free acid 6d.