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   <subfield code="a">Heteroorganic betaines</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="b">Reactions of betaines containing the+P−C−Si−S− fragment</subfield>
   <subfield code="c">[I. Borisova, N. Zemlyanskii, A. Shestakova, V. Khrustalev, Yu. Ustynyuk, E. Chernyshev]</subfield>
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   <subfield code="a">The [Ph3P+−CMe2−SiMe2−SEt]Br− salt was prepared by the reaction of betaine Ph3P+−CMe2SiMeR−S− (1a: R=Me) with EtBr. Acetylation of betaine1a or Et3P+−CHMeSiMe2−S− (2a) afforded 2,2,6-trimethyl-1,3-dioxa-2-silacyclohex-5-ene-4-thione or the [Et3P+−CHMeSiMe2Cl]Cl− salt depending on the reagent ratio. The reactions of betaines1a, b (1b: R=Ph) or2 with compounds (R3Sn)2X (X=O or NMe) can be used for the generation of silanones [RMeSi=O] and silaneimines [RMeSi=NMe] in solutions. The reactivity of betaines Ph3P+−CHR1SiMeR2−S− (R1=H or Me and R2=Me or Ph) is determined by the equilibrium between the zwitterionic and ylide Ph3P=CR1SiMeR2SH tautomers that exist in solutions.</subfield>
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   <subfield code="a">silicon-containing organophosphorus betaines</subfield>
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