Nucleophilic Reactions between Cyclic 1,2-Sulfites and Chloride Ions.
نویسندگان
چکیده
منابع مشابه
Reactions of enantiopure cyclic diols with sulfuryl chloride.
Monocyclic allylic cis-1,2-diols reacted with sulfuryl chloride at 0 °C in a regio- and stereo-selective manner to give 2-chloro-1-sulfochloridates, which were hydrolysed to yield the corresponding trans-1,2-chlorohydrins. At -78 °C, with very slow addition of sulfuryl chloride, cyclic sulfates were formed in good yields, proved to be very reactive with nucleophiles and rapidly decomposed on at...
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The potential energy surfaces for the reaction between H2O and the protonated alcohols MeOH2+, EtOH2+, PriOH2+, and Bu(t)OH2+ have been explored by means of high level ab initio theoretical methods. Both nucleophilic substitution (SN2) and elimination (E2) pathways have been investigated. Front side (SNF) and the familiar back side (SNB) Walden inversion attack of the nucleophile have been foun...
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ژورنال
عنوان ژورنال: Acta Chemica Scandinavica
سال: 1996
ISSN: 0904-213X
DOI: 10.3891/acta.chem.scand.50-0832