Abstract: trans-N-(Arenesulfonyl)-2-tributylstannyloxazolidines derived from (R)-phenylglycinol were diastereoselectively ring-opened by soft organometallic reagents in the presence of BF(3).OEt(2). Both higher order organocuprates and allyltributyltin afforded the desired products in good-to-excellent yields and high diastereoselectivities (dr up to 99/1). The stereochemical assignments of tributylstannyl-beta-aminoalcohols were firmly established from NMR data and after determination of several radiocrystallographic structures. Mechanisms were proposed in order to rationalize the observed selectivities.
Abstract: The preparation of polymer-supported allyltin reagents was shown to be possible for both unfunctionalized and functionalized allyl units. These reagents were treated with aldehydes in the presence of cerium(III) or indium(III) salts to afford high yields of homoallylic alcohols, practically uncontaminated with organotin residues (less than 5 ppm). Some mechanism aspects are briefly discussed and the potential for regeneration and reuse of these supported reagents is pointed out.
Abstract: [reaction: see text] Polymer-supported triorganotin halides were used in the halogenation reaction of aromatic amines. Treatment of aromatic amines with n-butyllithium and polymer-supported organotin halides gave the corresponding polymer-bound N-triorganostannylamines, which by treatment with bromine or iodine monochloride gave the para-halogenated aromatic amines with high yields and high selectivities. The polymer-supported organotin halides reagents regenerated during the course of the halogenation reaction can be reused without loss of efficiency. The presence of tin residues in halogenated aromatic amines was also investigated and evaluated at under 20 ppm after three runs.
Abstract: gamma-siloxyallyltributylstannanes were selectively obtained as E or Z isomers from beta-tributylstannylacrolein upon reaction with lithium or magnesium alkylcyanocuprates. The ability of the reagents to give a high syn selectivity when added to iminium salts has been used for the efficient synthesis of (+/-)-1-deoxy-6,8a-di-epi-castanospermine from succinimide. The key step of the synthesis was the allylstannation of the N-allyliminium intermediate followed by ring closing metathesis.
Abstract: Seventeen-electron compounds of MoIII having the general formula [(eta5-C5R5)Mo(eta4-diene)X2] (R = H, Me: dieney = butadiene, isoprene, or 2,3-dimethylbutadiene: X= Cl, CH3) are a new class of ethylene polymerization catalysts. The polyethylene obtained shows a bimodal distribution, the major weight fraction being characterized by very long (M around 10(6)) and highly linear polymer chains. The newly prepared pentamethylcyclopentadienyl (Cp*) derivatives are more active than the cyclopentadienyl (Cp) derivatives, but much less active than previously investigated niobiumIII compounds having the same stoichiometry. On the other hand, the turnover frequency of the active site leading to the high molecular weight chains is at least 10 times greater than that obtained with the corresponding Nb catalyst. The reason for the low activity is explained by a difficult activation process that is attributed to the low polarity and high strength of the Mo-alkyl bond. This is confirmed by a Mulliken charge analysis of density functional theory (DFT) geometry-optimized [CpM(eta4-C4H6)(CH3)2] (M = Nb, Mo) and by the calculation of the heterolytic bond dissociation energies. DFT calculations have also been carried out on the ethylene insertion coordinate for the [CpM(eta4-C4H6)(CH3)]+ model of the presumed active site. The results indicate an equivalent activation barrier to insertion for the Nb and Mo systems. Differences in optimized geometries for the reaction intermediates are attributed to the presence of the extra electron for the Mo system. This electron opposes the formation of M-H-C agostic interactions, while it strengthens the back-bonding M-ethylene interaction, but otherwise plays no active role in the polymer chain propagation mechanism. According to the calculations, the chain propagation for the Mo system occurs entirely on the spin doublet surface, the minimum energy crossover point with the quartet surface lying at a higher energy than the transition state for insertion on the doublet surface.
Abstract: Density functional calculations of bond dissociation energies (BDEs) have been used as a guide to the choice of metal system suitable for controlling styrene polymerization by either the stable free radical polymerization (SFRP) or the atom transfer radical polymerization (ATRP) mechanism. In accord with the theoretical prediction, CpMo(eta(4)-C(4)H(6))(CH(2)SiMe(3))(2), 2, is not capable of yielding SFRP of styrene. Still in accord with theoretical prediction, CpMo(eta(4)-C(4)H(6))Cl(2), 1, CpMo(PMe(3))(2)Cl(2), 3, and CpMo(dppe)Cl(2) (dppe = 1,2-bis(diphenylphosphino)ethane), 4, yield controlled styrene polymerization by the SFRP mechanism in the presence of 2,2'-azobisisobutyronitrile (AIBN). This arises from the generation of a putative Mo(IV) alkyl species from the AIBN-generated radical addition to the Mo(III) compound. The controlled nature of the polymerizations is indicated by linear M(n) progression with the conversion in all cases and moderate polydispersity indices (PDIs). Controlled polymerization of styrene is also given by compounds 3 and 4 in combination with alkyl bromides. These complexes then operate by the ATRP mechanism, again in accord with the theoretical predictions. Controlled character is revealed by linear increase of M(n) versus conversion, low PDIs, a stop-and-go experiment, and (1)H NMR and MALDI-TOF analyses of the polymer end groups. The same controlled polymerization is given by a "reverse" ATRP experiment, starting from AIBN and CpMo(PMe(3))(2)Cl(2)Br, 5. On the other hand, when compound 1 or 2 is used in combination with an alkyl bromide (as for an ATRP experiment), the isolated polystyrene shows by M(n), (1)H NMR, and MALDI-TOF analyses that catalytic chain transfer (CCT) radical polymerization takes place in this case. Kinetics simulations underscore the conditions regulating the radical polymerization mechanism and the living character of the polymerization. The complexes herein described are ineffective at controlling the polymerization of methyl methacrylate.
