Answers are grounded in this paper and cite their sources.
In this account we review the varied, but extensively documented reactions affording acyclic alkanesulfonates, alkanesulfonamides, and heterocyclic ring systems (sultones, 1,2‐oxathiole S , S ‐dioxides, sultams, and 2,3‐dihydroisothiazole S , S ‐dioxides) from conveniently functionalized alkanesulfonates or alkanesulfonamides, by a general procedure that we have named and classified as CSIC reactions both as intermolecular [ C arbanion‐mediated S ulfonate (or S ulfonamide) I ntermolecular C oupling] and as intramolecular [ C arbanion‐mediated S ulfonate (or S ulfonamide) I ntramolecular C yclization] variants of the conversion. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
No takes yet. Share an insight, caveat, or question.
Postel et al. (2003) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: