Abstract
It has been found that the nucleophilic ring-opening of epoxides by arenesulfinates, in the presence of magnesium nitrate as a Lewis acid catalyst, provides a preparatively useful, convenient route to β-hydroxysulfones.
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 12, 1982 - Issue 14
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Related Research Data
Synthesis of β-hydroxysulfones through a copper(II)-catalyzed multicomponent reaction with the insertion of sulfur dioxide
Source:
Royal Society of Chemistry (RSC)
Aerobic Oxysulfonylation of Alkenes Leading to Secondary and Tertiary β‐Hydroxysulfones
Source:
Wiley
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