Boron-containing side products

Acylation of 3-substituted indoles is more difficult, however 2-acetylation can be effected with the aid of boron trifluoride catalysis." " Indoles, with a carboxyl-containing side-chain acid at C-3, undergo intramolecular acylation forming cyclic 2-acylindoles." Intramolecular Vilsmeier processes, using tryptamine amides, have been used extensively for the synthesis of 3,4-dihydro-p-carbolines, a sub-structure found in many indole alkaloids (P-carboline is the widely used, trivial name for pyrido[3,4-fc]indole). Note that it is the imine, rather than a ketone, that is the final product the cyclic nature of the imine favours its retention rather than hydrolysis to amine plus ketone as in the standard Vilsmeier sequence " this ring closure is analogous to the Bischler-Napieralski synthesis of 3,4-dihydro-isoquinolines (9.15.1.7). 

The insertions of olefins into metal-silyl complexes is an important step in the hydrosi-lylation of olefins, and the insertions of olefins and alkynes into metal-boron bonds is likely to be part of the mechanism of the diborations and sUaborations of substrates containing C-C multiple bonds. Other reactions, such as the dehydrogenative sUylation of olefins can also involve this step. Several studies imply that the rhodium-catalyzed hydrosilylations of olefins occur by insertion of olefins into rhodium-silicon bonds, while side products from palladium- and platinum-catalyzed hydrosilylations are thought to form by insertion of olefins into the metal-sihcon bonds. In particular, vinylsilanes are thought to form by a sequence involving olefin insertion into the metal-silicon bond, followed by p-hydrogen elimination (Chapter 10) to form the metal-hydride and vinylsilane products. 

Nitrogen triiodide also forms through an ozonation reaction of K1 in an aqueous solution of ammonia (product contains NHI2 and NH2I side products) [67]. Formation of gaseous NI3 was observed in the case of reaction of boron nitride with iodine monofluoride [52]. 

S.3.2 Via Mannich-Type Reaction. Hattori et al.42 used a Mannich-type reaction for constructing the taxol side chain. In the presence of a BINOL-containing boron compound, the asymmetric Mannich reaction proceeded smoothly, providing the product with good yield (Scheme 7-86). 

Ceramic-type materials that contain no organic linkage units can be prepared by the pyrolysis of cyclic or high polymeric aminophosphazenes. An example is shown in reaction (44). Under appropriate conditions, pyrolysis products that correspond to phosphorus-nitride are formed. Polyphosphazenes that contain both amino and borazine side groups yield phosphorus-nitrogen-boron ceramics following pyrolysis 94,95 The conversion of a formable polymer into a ceramic has many potential advantages for the controlled synthesis and fabrication of advanced ceramics. This principle is discussed in more detail in Chapter 9. 

Kaneka has proposed flame retardants containing both silicon and boron, such as the reaction product of phenyl trichlorosilane and boric acid. Borealis has patented a polyolefin wire and cable composition containing metal hydroxides and a small quantity of an organosiloxane containing methyl, phenyl, vinyl or similar side-groups. 

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