Asymmetric synthesis and applications of beta-amino Weinreb amides: asymmetric synthesis of (S)-coniine.

Conjugate addition of lithium (S)-N-benzyl-N-alpha-methylbenzylamide to a range of alpha, beta-unsaturated Weinreb amides proceeds with high levels of diastereoselectivity (>95% de). The beta-amino Weinreb amide products may be transformed into beta-amino ketones via reactions with Grignard reagents, while treatment with DIBAL-H furnishes beta-amino aldehydes. Trapping of the aldehyde via Wadsworth-Emmons reaction and subsequent manipulation offers an efficient route to homochiral delta-amino acid derivatives and 2-substituted piperidines. The application of this methodology for the synthesis of (S)-coniine is demonstrated.

[1]  R. Pedrosa,et al.  A Simple Stereoselective Synthesis of Enantiopure 2‐Substituted Pyrrolidines and Piperidines from Chiral (R)‐Phenylglycinol‐Derived Bicyclic 1,3‐Oxazolidines , 2000 .

[2]  M. Mckervey,et al.  Convenient in Situ Synthesis of Nonracemic N-protected β-Amino Aldehydes from β-Amino Acids. Applications in Wittig Reactions and Heterocycle Synthesis , 1999 .

[3]  C. Escolano,et al.  Enantioselective synthesis of piperidine, indolizidine, and quinolizidine alkaloids from a phenylglycinol-derived delta-lactam. , 2003, The Journal of organic chemistry.

[4]  Tianan Fang,et al.  δ-Amino β-Keto Esters, a Designed Polyfunctionalized Chiral Building Block for Alkaloid Synthesis. Asymmetric Synthesis of (R)-(+)-2-Phenylpiperidine and (−)-SS20846A , 2000 .

[5]  S. Graham,et al.  A new mode of reactivity of N-methoxy-N-methylamides with strongly basic reagents , 1990 .

[6]  O. Ichihara,et al.  Asymmetric synthesis of (−)-(1R,2S)-cispentacin and related cis- and trans-2-amino cyclopentane- and cyclohexane-1-carboxylic acids , 1994 .

[7]  O. Ichihara,et al.  Asymmetric syntheses of β-phenylalanine, α-methyl-β-phenylalanines and derivatives , 1993 .

[8]  B. E. Evans,et al.  A synthesis of statine utilizing an oxidative route to chiral .alpha.-amino aldehydes , 1982 .

[9]  O. Ichihara,et al.  Asymmetric synthesis of R-β-amino butanoic acid and S-β-tyrosine: Homochiral lithium amide equivalents for Michael additions to α,β-unsaturated esters. , 1991 .

[10]  G. E. Keck,et al.  Some unusual reactions of weinreb amides , 1993 .

[11]  S. Davies,et al.  Asymmetric synthesis of anti-α-alkyl-β-amino acids , 1994 .

[12]  J. Bosch,et al.  Chiral precursors for the synthesis of enantiomerically pure piperidines. Total synthesis of (R)-(-)-coniine , 1994 .

[13]  O. Ichihara,et al.  An Expeditious Asymmetric Synthesis of (-)-(1R,2S) -Cispentacin , 1993 .

[14]  M. Grenon,et al.  Practical and highly regio- and stereoselective synthesis of 2-substituted dihydropyridines and piperidines: application to the synthesis of (-)-coniine. , 2001, Journal of the American Chemical Society.

[15]  M. Reetz Synthesis and diastereoselective reactions of n,n-dibenzylamino aldehydes and related compounds. , 1999, Chemical reviews.

[16]  J. Celerier,et al.  New highly enantioselective synthesis of 6-alkylpiperidin-2-ones and 2-substituted piperidines , 1995 .

[17]  Hisashi Yamamoto,et al.  Asymmetric aza-Diels-Alder reaction : enantio- and diastereoselective reaction of imine mediated by chiral Lewis acid , 1993 .

[18]  S. Davies,et al.  Asymmetric syntheses of moiramide B and andrimid , 1998 .

[19]  Yong Hae Kim,et al.  Diastereoselective addition of organolithiums to new chiral hydrazones. Enantioselective synthesis of (R)-coniine , 1996 .

[20]  S. Nahm,et al.  N-methoxy-n-methylamides as effective acylating agents , 1982 .

[21]  J. Smialek,et al.  Clinical spectrum of accidental hemlock poisoning: neurotoxic manifestations, rhabdomyolysis and acute tubular necrosis. , 1991, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[22]  I. Markó,et al.  Synthetic Approaches Towards Manzamine. An easy preparation of β-amino Aldehydes , 1990 .

[23]  S. Davies,et al.  Syntheses of derivatives of L-daunosamine and its C-3 epimer employing as the key step the asymmetric conjugate addition of a homochiral lithium amide to tert-butyl (E,E)-hexa-2,4-dienoate , 1999 .

[24]  K. Rodriques A novel route to cyclopropyl ketones, aldehydes, and carboxylic acids. , 1991 .

[25]  O. Ichihara,et al.  Asymmetric synthesis of (+)-negamycin , 1996 .

[26]  O. Ichihara,et al.  A Succinct Asymmetric Synthesis of (2S,3R)-2-Methyl-3-aminopentanoic Acid Hydrochloride , 1994 .

[27]  O. Ichihara,et al.  Asymmetric synthesis of syn-α-alkyl-β-amino acids , 1994 .

[28]  M. Munchhof,et al.  An Asymmetric Route to Chiral, Nonracemic 2-Substituted Piperidines. Synthesis of (-)-Pipecoline, (+)-Coniine, and (-)-Coniceine , 1995 .

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

[30]  T. J. Wilkinson,et al.  Enantioselective syntheses of 2-alkyl- and 2,6-dialkylpiperidine alkaloids: preparations of the hydrochlorides of (-)-coniine, (-)-solenopsin A, and (-)-dihydropinidine. , 2000, Organic letters.

[31]  D. Enders,et al.  A New Asymmetric Synthesis of both Enantiomers of Coniine by 1,2‐Addition of RLi/YbCl3 to Aldehyde SAMP Hydrazones , 1993 .

[32]  C. Bochet,et al.  Diastereo- and enantioselective syntheses of (−)-coniine, (−)-solenopsin A, (−)-solenopsis fugaz venom and (−)-xenovenine via deoxygenative decarboxylation of 2-carbonylsultam-substituted n-hydroxy-piperidines and -pyrrolidines , 1994 .

[33]  K. Prasad,et al.  N-Sulfinyl β-Amino Weinreb Amides: Synthesis of Enantiopure β-Amino Carbonyl Compounds. Asymmetric Synthesis of (+)-Sedridine and (−)-Allosedridine , 2003 .

[34]  F. A. Davis,et al.  Synthesis and applications of nonracemic β-amino aldehydes to the asymmetric synthesis of piperdines: (+)-dihydropinidine , 1998 .

[35]  C. W. Jefford,et al.  An enantiospecific synthesis of solenopsin A , 1993 .

[36]  A. Katritzky,et al.  Efficient Routes to Chiral 2-Substituted and 2,6-Disubstituted Piperidines , 1998 .

[37]  M. Bunnage,et al.  An expeditious asymmetric synthesis of allophenylnorstatine , 1994 .

[38]  O. Ichihara,et al.  Asymmetric synthesis of N-protected syn and anti (E)-3-amino-2-hydroxy-4-hexenoate: A practical method for the C-α epimerization of anti β-amino-α-hydroxy acids , 1999 .

[39]  C. Kibayashi,et al.  Total syntheses of (+)-castanospermine and (+)-1-epicastanospermine and their 1-O-acyl derivatives from a common chiral building block , 1993 .

[40]  D. Perrone,et al.  2-Thiazolyl α-Amino Ketones: A New Class of Reactive Intermediates for the Stereocontrolled Synthesis of Unusual Amino Acids , 2010 .

[41]  R. Al-awar,et al.  Conversion of N-acyl-2,3-dihydro-4-pyridones to 4-chloro-1,2-dihydropyridines using the Vilsmeier reagent. Synthesis of (-)-coniine and (±)-lupinine , 1993 .

[42]  U. Jacobsson,et al.  High pressure approach to the total synthesis of 6-EPI-d-purpurosamine b , 1987 .

[43]  Y. Hirai,et al.  Construction of chiral 2-functionalized piperidine via enzymatic resolution and palladium-catalyzed N-alkylation , 1994 .