Highly regio- and stereoselective iodocyclization of chiral 3-alkoxycarbonyl-4-propenyl-2,2-dimethyl-1,3-oxazolidines: a computational investigation
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[1] A. Kakehi,,et al. A facile and regio- and stereo-selective preparation of bicyclic guanidines by iodocyclization of 3-(alk-2-enyl)-2-(substituted amino)-1-imidazolin-4-ones , 1996 .
[2] P. Herdewijn,et al. Branched-chain nucleosides: Synthesis of 3′-deoxy-3′-C- hydroxymethyl-α-l-lyxopyranosyl thymine and 3′-deoxy- 3′-C-hydroxymethyl-α-l-threofuranosyl thymine. , 1996 .
[3] J. A. Marshall,et al. Stereoselective Synthesis of Differentially Protected Derivatives of the Higher Amino Sugars Destomic Acid and Lincosamine from Serine and Threonine. , 1996, The Journal of organic chemistry.
[4] F. Zanardi,et al. General approach to hydroxylated α-amino acids exploiting N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole , 1994 .
[5] H. Schlegel,et al. Combining Synchronous Transit and Quasi-Newton Methods to Find Transition States , 1993 .
[6] P. Beaulieu,et al. Synthesis of chiral vinylglycines , 1991 .
[7] W. Hehre,et al. Modeling chemical reactivity. 7. The effect of a change in rate-limiting step on the stereoselectivity of electrophilic addition to allylic alcohols and related chiral alkenes , 1987 .
[8] A. Bongini,et al. Iodocyclofunctionalization of (E)-1-trichloroacetimidoalk-2-enes. Synthesis of (±)-erythro-sphinganine triacetate , 1986 .
[9] H. Pauls,et al. A novel synthesis of methyl .alpha.-L-garosaminide which illustrates a stereocontrolled approach to the cis-hydroxyamino moiety of amino sugars , 1980 .