Trimethylsilyl groups, heterocyclic

These two compounds 1 and 2 cannot always be considered as synthetic equivalents of diazomethane for example, they do not react with carboxylic acids to give esters. In fact, they play a very different role in synthesis, and it is demonstrated in this review that they are powerful synthetic building blocks. Since tin chemistry is often compared to that of silicon, a few results involving bis(trimethylstannyl)diazomethane 3 [4] will also be presented (Scheme 1). Juggling the relative steric bulk of the triisopropylsilyl versus the trimethylsilyl group, and the enhanced reactivity of tin-carbon compared to silicon-carbon bonds, the three diazomethane derivatives 1-3 are complementary synthons. Not only are they attractive precursors for the synthesis of stable compounds hitherto believed to be only transient intermediates, but also of new heterocycles or even of polymer crosslinking agents. 

In 2002, Leadbeater and Torenius reported the base-catalyzed Michael addition of methyl acrylate to imidazole using ionic liquid-doped toluene as a reaction medium (Scheme 6.133 a) [190], A 75% product yield was obtained after 5 min of microwave irradiation at 200 °C employing equimolar amounts of Michael acceptor/donor and triethylamine base. As for the Diels-Alder reaction studied by the same group (see Scheme 6.91), l-(2-propyl)-3-methylimidazolium hexafluorophosphate (pmimPF6) was the ionic liquid utilized (see Table 4.3). Related microwave-promoted Michael additions studied by Jennings and coworkers involving indoles as heterocyclic amines are shown in Schemes 6.133 b [230] and 6.133 c [268], Here, either lithium bis(trimethylsilyl)amide (LiHMDS) or potassium tert-butoxide (KOtBu) was em-... 

Al-Sb heterocycles were obtained for the first time in our group from reactions of dialkylalanes R2A1H and tris(trimethylsilyl)stibine Sb(SiMe3)3. 

Another type of adducts [8, Eq. (3)] was formed by the reaction of di(fert-butyl)aluminum chloride with dilithium bis(trimethylsilyl)hydrazide in low yields below 30% [19]. The structure of 8 consists of a distorted heterocubane with four vertices occupied by nitrogen atoms, two of which are connected by an intact N—N bond across one face of the cube. The cation positions are occupied by two aluminum and two lithium atoms, of which the last ones bridge the N—bond. Part of the hydrazide molecules was cleaved, and the aluminum atoms are bonded to one ferf-butyl group only. On the basis of the NMR spectroscopic characterization many unknown by-products were formed in the course of that reaction, and no information is available concerning the reaction mechanism. Compound 8 may be described as an adduct of dilithium bis(trimethylsilyl)hydrazide to a dimeric iminoalane containing a four-membered AI2N2 heterocycle. Further... 

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