Trimethylene thioacetals

Trimethylene dithiotosylate, 539-540 Trimethylene thioacetals, 79 Trimethyl orthoacetate, 565 Trimethyl orthoformate, 540... 

The difficulties encountered in the regeneration of steroidal ketones from their ethylene or trimethylene thioacetals by the mercury(n) salt procedure have been circumvented 1-chlorobenzotriazole smoothly oxidizes thioacetals to the corresponding disulphoxides, which, without isolation, furnish the desired ketones in satisfactory yield on treatment with aqueous base. 

As described in the previous section, a-elimination of dialkyltitanocenes is of limited use for the preparation of titanocene-alkylidenes. Since thioacetals are readily available from carbonyl compounds or through alkylation of bis(phenylthio)methane and related organosulfur compounds, a thioacetal-titanocene(II) system enables the use of different types of carbene complexes. Use of appropriate thioacetals is of crucial importance in this system for the preparation of alkylidene complexes 48, the corresponding diphenyl thioacetals are the starting materials of choice. No carbene complexes are formed from dialkylthio-acetals. To generate vinylcarbene complexes 49, trimethylene thioacetals of aji-unsaturated aldehydes or l,3-bis(phenylthio)propene derivatives are employed (Scheme 4.41). The low-valent titanium species 44 is also easily prepared by the reduction of titanocene dichloride with magnesium in the presence of triethyl phosphite at room temperature. The presence of molecular sieves 4A is essential for the reproducibility of this preparation. In relatively large-scale preparations, care should be taken to control the reaction temperature [92, 93g]. 

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