Reduction of 2-acylaziridines by samarium(II) iodide. An efficient and regioselective route to β-amino carbonyl compounds

[1]  L. Overman,et al.  Stereocontrolled Total Syntheses of meso-Chimonanthine and meso-Calycanthine via a Novel Samarium Mediated Reductive Dialkylation , 1996 .

[2]  I. Kawasaki,et al.  Reductive Dimerization of Cyclopropane-1,1-dicarboxylic Esters Using Samarium(II) Diiodide (SmI2) , 1996 .

[3]  R. Little,et al.  Asymmetric Reductive Cyclization. Total Synthesis of (−)-C10-Desmethyl Arteannuin B , 1996 .

[4]  J. Marco-Contelles,et al.  Cleavage of N−O Bonds Promoted by Samarium Diiodide: Reduction of Free or N-Acylated O-Alkylhydroxylamines , 1996 .

[5]  Y. Lim,et al.  Regiospecific reductive ring cleavage of N-substituted aziridine-2-carboxylates and an aziridine-2-methanol via catalytic hydrogenation using Pd as a catalyst , 1995 .

[6]  Travis T Wager,et al.  Reductive cleavage of NO bonds in hydroxylamine and hydroxamic acid derivatives using SmI2/THF , 1995 .

[7]  G. Molander,et al.  REDUCTION OF 2-ACYLAZIRIDINES BY SAMARIUM(II) IODIDE. AN EFFICIENT AND REGIOSELECTIVE ROUTE TO BETA -AMINO KETONES AND ESTERS , 1995 .

[8]  J. Marco-Contelles,et al.  Intramolecular reductive coupling of carbonyl-tethered oxime ethers promoted by samarium diiodide: A powerful method for the stereoselective synthesis of aminocyclopentitols , 1995 .

[9]  T. Horaguchi,et al.  Reactions of 1-bromo-2,3-epoxypropane with samarium diiodide: First observation of carbon-carbon bond cleavage of oxiranylmethyl radical under the single electron transfer conditions , 1995 .

[10]  G. E. Keck,et al.  TOTAL SYNTHESIS OF (+)-7-DEOXYPANCRATISTATIN : A RADICAL CYCLIZATION APPROACH , 1995 .

[11]  S. Davies,et al.  An Asymmetric Synthesis of N-Protected β-Amino Aldehydes and β-Amino Ketones , 1995 .

[12]  J. Liebscher,et al.  Enantioselective synthesis of hydroxyethyloxiranecarboxylic acid derivatives by epoxidation of 5-ylidene-1,3-dioxane-4-ones , 1995 .

[13]  I. Kawasaki,et al.  Ring opening of cyclopropanecarboxylates using samarium(II) diiodide (SmI2)-HMPA-THF system , 1995 .

[14]  S. Danishefsky,et al.  Total Synthesis of (.+-.)-FR-900482 , 1995 .

[15]  E. Enholm,et al.  TETRAHYDROPYRAN RING-OPENING REACTIONS PROMOTED BY SMI2 , 1995 .

[16]  D. W. Young,et al.  Synthesis of α-amino acids by ring opening of aziridine-2-carboxylates with carbon nucleophiles , 1995 .

[17]  E. Vedejs,et al.  Deprotection of Arenesulfonamides with Samarium iodide , 1994 .

[18]  D. Tanner Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations , 1994 .

[19]  Wei Wang,et al.  Conversion of .beta.-amino esters to .beta.-lactams via tin(II) amides , 1993 .

[20]  C. Schofield,et al.  Amino acid synthesis via ring opening of N-sulphonyl aziridine-2-carboxylate esters with organometallic reagents , 1993 .

[21]  M. Faul,et al.  Bis(oxazoline)-copper complexes as chiral catalysts for the enantioselective aziridination of olefins , 1993 .

[22]  Chris P. Miller,et al.  An investigation of the mitsunobu reaction in the preparation of peptide oxazolines, thiazolines, and aziridines , 1992 .

[23]  Yong Hae Kim,et al.  Reductive ring opening of cyclopropyl ketones with samarium (II) diiodide , 1992 .

[24]  J. H. Boom,et al.  One-step synthesis of optically active benzyl N-trityl-L-aziridine-2-carboxylic esters , 1992 .

[25]  M. Faul,et al.  Copper-catalyzed aziridination of olefins by (N-(p-toluenesulfonyl)imino)phenyliodinane , 1991 .

[26]  G. Molander,et al.  A facile synthesis of bicyclo[m.n.1]alkan-1-ols. Evidence for organosamarium intermediates in the samarium(II) iodide promoted intramolecular Barbier-type reaction , 1991 .

[27]  M. Hashimoto,et al.  SYNTHESIS OF OPTICALLY ACTIVE β-METHYLTRYPTOPHANS FROM AZIRIDINE-2-CARBOXYLATES , 1990 .

[28]  O. Meth–Cohn,et al.  A stereocontrolled approach to electrophilic epoxides , 1988 .

[29]  G. Molander,et al.  Lanthanides in organic synthesis. 5. Reduction of vinyloxiranes with samarium diiodide. An efficient route to functionalized chiral, non-racemic (E)-allylic alcohols , 1986 .

[30]  G. Molander,et al.  Lanthanides in organic synthesis. 4. Reduction of .alpha.,.beta.-epoxy ketones with samarium diiodide. A route to chiral, nonracemic aldols , 1986 .

[31]  C. Sha,et al.  Intramolecular 1,3-dipolar cycloaddition of alkyl azide enones and rearrangements of the triazoline intermediates. Formal total synthesis of (±)-desamylperhydrohistrionicotoxin , 1986 .

[32]  K. Nakajima,et al.  Studies on 2-Aziridinecarboxylic Acid. IV. Total Synthesis of Actinomycin D (C1) via Ring-opening Reaction of Aziridine , 1980 .

[33]  D. Cole Recent stereoselective synthetic approaches to β-amino acids , 1994 .

[34]  M. Reetz,et al.  Stereoselective epoxidation of chiral electron-poor γ-aminoolefins , 1991 .

[35]  C. Schofield,et al.  The ring opening of aziridine-2-carboxylate esters with organometallic reagents , 1989 .

[36]  A. Kozikowski,et al.  Construction of optically pure tryptophans from serine derived aziridine-2-carboxylates , 1989 .

[37]  H. Terano,et al.  Structure and synthesis of FR900490, a new immunomodulating peptide isolated from a fungus , 1988 .

[38]  J. Baldwin,et al.  Nucleophilic ring opening of aziridine-2-carboxylates with Wittig reagents; an enantioefficient synthesis of unsaturated amino acids , 1987 .

[39]  J. Inanaga,et al.  SmI2-Induced highly regioselective reduction of α,β-epoxy esters and γ,δ-epoxy-α,β-unsaturated esters. An efficient route to optically active β-hydroxy and δ-hydroxy esters , 1987 .

[40]  John A. Murphy,et al.  Novel synthesis of vinyl ethers induced by carbon–halogen bond homolysis , 1986 .