Stereoselectivity in oxyallyl–furan (4 + 3) cycloadditions: control of intermediate conformations and dispersive stabilisation in cycloadditions involving oxazolidinone auxiliaries
نویسندگان
چکیده
منابع مشابه
DFT Studies on the Stereoselectivity of α-Silyloxy Diazoalkane Cycloadditions.
The intramolecular [3+2] cycloaddition (32CA) of alkene-tethered α-silyloxydiazoalkanes provides variable stereoselectivity in generating bicyclic pyrazolines where the silyloxy group is either syn or anti to the newly formed pyrazoline ring. To elucidate the origin of the stereoselectivity, density functional theory (DFT) calculations were carried out for the energy of each transition state st...
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Staudinger reactions of Cy2BN3 with tri-substituted phosphines (R3P) yielded the boron-nitrogen-phosphorus linked systems Cy2BN=PR3 (R = Et, (t)Bu, Cy, Ph) (1a-1d respectively). Similarly, reaction of (C6F5)2BN3 with the phosphines P(t)Bu3, PPh3, Ph2PC≡CPh and Ph2PC≡CPPh2 yielded (C6F5)2BN=PR3 (2a-d respectively). In contrast, the reaction of (C6F5)2BN3 with Ph2P-C≡Cp-tol in the presence of exc...
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Iridium-catalyzed intramolecular [4 + 2] cycloadditions of diene-tethered alkynyl halides were investigated by using [IrCl(cod)](2) as catalyst, and dppe was found to be the most suitable phosphine ligand for the reaction. No oxidative insertion of the iridium into the carbon-halide bond was observed, and the reactions proceeded to provide the halogenated cycloadducts in good yield (75-94%). Th...
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ژورنال
عنوان ژورنال: Chemical Science
سال: 2010
ISSN: 2041-6520,2041-6539
DOI: 10.1039/c0sc00280a