Stereo- and regioselective ring opening of alkenyl aziridines with metal halides
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[1] G. Righi,et al. Stereocontrolled ‘one pot’ organometallic addition–ring opening reaction of α,β-aziridine aldehydes. A new entry to syn 1,2-amino alcohols , 2001 .
[2] G. Righi,et al. Stereo- and regiocontrolled transformations of vinyloxiranes with metal halides , 2000 .
[3] G. Righi,et al. An Easy Deoxygenation of Conjugated Epoxides , 2000 .
[4] G. Righi,et al. A mild preparation of a-halo-a,-enones from cyclic enones , 1999 .
[5] B. Bonini,et al. Allylation reactions of acylsilanes as synthetic equivalents of aldehydes. Application to a stereocontrolled synthesis of (1S,2S,5S)-(10S)-and-(10R)-allyl myrtanol , 1998 .
[6] G. Righi,et al. Highly regioselective opening of optically active N-Boc-2,3-aziridino alcohol derivatives with metal halides , 1998 .
[7] G. Righi,et al. Metal halide-mediated opening of three membered rings: enantioselective synthesis of (2S,3R)-3-amino-2-hydroxydecanoic acid and (3R)-3-aminodecanoic acid , 1997 .
[8] R. Racioppi,et al. Unprecedented biocatalytic desymmetrization of hexitols , 1997 .
[9] H. Tamamura. Regiospecific ring-opening reactions of aziridines bearing an α,β-unsaturated ester group with trifluoroacetic acid or methanesulfonic acid: application to the stereoselective synthesis of (E)-alkene dipeptide isosteres , 1997 .
[10] P. Somfai,et al. Synthesis and Aza-[2,3]-Wittig Rearrangements of Vinylaziridines: Scope and Limitations. , 1996, The Journal of organic chemistry.
[11] B. Bonini,et al. Highly Stereoselective Route toward the Synthesis of beta- and gamma-Amino Alcohols from Homochiral alpha- and beta-Amino Acylsilanes as Synthetic Equivalents of alpha- and beta-Amino Aldehydes. , 1996, The Journal of organic chemistry.
[12] G. Righi,et al. Regioselective opening of 3-Substituted N-Ethoxycarbonyl aziridine-2-carboxylates with metal halides toward the preparation of α and β-amino acids , 1996 .
[13] G. Righi,et al. Stereoselective Preparation of Syn α-Hydroxy-β-amino Ester Units via Regioselective Opening of α,β-Epoxy Esters: Enantioselective Synthesis of Taxol C-13 Side Chain and Cyclohexylnorstatine , 1996 .
[14] G. Righi,et al. Synthesis of the C1C10 fragment of the macrolide antibiotic Nystatin A1 from a chiral building block obtained via chemoenzymatic approach , 1996 .
[15] L. Rossi,et al. C-1 Reactivity of 2,3-Epoxy Alcohols via Oxirane Opening with Metal Halides: Applications and Synthesis of Naturally Occurring 2,3-Octanediol, Muricatacin, 3-Octanol, and 4-Dodecanolide , 1995 .
[16] P. Wipf,et al. SN2'-Reactions of Peptide Aziridines. A Cuprate-Based Approach to (E)-Alkene Isosteres , 1994 .
[17] A. Scettri,et al. A new procedure for Horner-Wadsworth-Emmons olefination of carbonyl compounds , 1994 .
[18] D. Tanner. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations , 1994 .
[19] P. Deslongchamps,et al. Stereoelectronic effects in organic chemistry , 1983 .