Total synthesis of (+)-galanthamine starting from d-glucose

[1]  T. Ōishi,et al.  Total synthesis of Amaryllidaceae alkaloids, (+)-vittatine and (+)-haemanthamine, starting from d-glucose , 2007 .

[2]  N. Camp,et al.  Stereocontrolled synthesis of (-)-galanthamine. , 2007, Organic letters.

[3]  Y. Hamashima,et al.  Biomimetic synthesis of (+/-)-galanthamine and asymmetric synthesis of (-)-galanthamine using remote asymmetric induction. , 2006, Chemical & pharmaceutical bulletin.

[4]  N. Chida,et al.  Total synthesis of actinobolin from d-glucose by way of the stereoselective three-component coupling reaction , 2006 .

[5]  Y. Tu,et al.  Total synthesis of (+/-)-galanthamine. , 2006, Organic letters.

[6]  J. Marco-Contelles,et al.  Synthesis and pharmacology of galantamine. , 2006, Chemical reviews.

[7]  B. Trost,et al.  Divergent enantioselective synthesis of (-)-galanthamine and (-)-morphine. , 2005, Journal of the American Chemical Society.

[8]  Y. Hamashima,et al.  Total synthesis of (-)-galanthamine by remote asymmetric induction. , 2004, Angewandte Chemie.

[9]  N. Chida,et al.  A new entry to Amaryllidaceae alkaloids from carbohydrates: total synthesis of (+)-vittatine. , 2004, Chemical Communications.

[10]  Ana M. Martin Castro,et al.  Claisen rearrangement over the past nine decades. , 2004 .

[11]  S. Lilienfeld.  Galantamine--a novel cholinergic drug with a unique dual mode of action for the treatment of patients with Alzheimer's disease. , 2006, CNS drug reviews.

[12]  B. Trost,et al.  An efficient enantioselective synthesis of (-)-galanthamine. , 2002, Angewandte Chemie.

[13]  S. Danishefsky,et al.  Explorations in organic chemistry leading to the total synthesis of (+/-)-gelsemine. , 2002, Journal of the American Chemical Society.

[14]  R. Ferrier.  Direct Conversion of 5,6-Unsaturated Hexopyranosyl Compounds to Functionalized Cyclohexanones , 2001 .

[15]  C. Guillou,et al.  An Efficient Total Synthesis of (±)-Galanthamine , 2001 .

[16]  Y. Hamashima,et al.  An efficient synthesis of (±)-narwedine and (±)-galanthamine by an improved phenolic oxidative coupling. , 2001, Angewandte Chemie.

[17]  N. Cutler,et al.  Review of the acetylcholinesterase inhibitor galanthamine , 2000, Expert opinion on investigational drugs.

[18]  U. Jordis,et al.  Development of a Pilot Scale Process for the Anti-Alzheimer Drug (−)-Galanthamine Using Large-Scale Phenolic Oxidative Coupling and Crystallisation-Induced Chiral Conversion , 1999 .

[19]  M. Weinstock,et al.  Selectivity of Cholinesterase Inhibition , 1999 .

[20]  D. Trauner,et al.  PRACTICAL SYNTHESIS OF (-)-MORPHINE , 1999 .

[21]  D. Trauner,et al.  Synthesis of Enantiomerically Pure Morphine Alkaloids: The Hydrophenanthrene Route. , 1998, The Journal of organic chemistry.

[22]  E. Giacobini.  Invited Review Cholinesterase inhibitors for Alzheimer’s disease therapy: from tacrine to future applications , 1998, Neurochemistry International.

[23]  Susan Budavari,et al.  The Merck index , 1998 .

[24]  D. Trauner,et al.  The phenanthrenone approach to opium alkaloids: Formal total synthesis of morphine by sigmatropic rearrangement , 1997 .

[25]  N. Chida,et al.  Chiral and stereoselective total synthesis of (-)-mesembranol starting from D-glucose , 1997 .

[26]  M. Rainer.  CLINICAL STUDIES WITH GALANTHAMINE , 1997 .

[27]  H. Mucke,et al.  Preclinical studies with galanthamine , 1997 .

[28]  T. Hashimoto,et al.  Synthesis of an enantiomerically pure aminoisoquinocarbazole with antiarrhythmic activity via lipase-catalyzed enantioselective transesterification , 1996 .

[29]  W. H. Pearson,et al.  An efficient synthesis of (±)-crinane using an intramolecular azide-olefin cycloaddition , 1996 .

[30]  P. Parsons,et al.  Tandem Reactions in Organic Synthesis: Novel Strategies for Natural Product Elaboration and the Development of New Synthetic Methodology. , 1996, Chemical reviews.

[31]  W. Shieh,et al.  Asymmetric Transformation of Either Enantiomer of Narwedine via Total Spontaneous Resolution Process, a Concise Solution to the Synthesis of (-)-Galanthamine , 1994 .

[32]  David R. Williams,et al.  Synthesis strategies for marine diterpenes. Total synthesis of the clavularanes , 1993 .

[33]  R. Ferrier,et al.  THE CONVERSION OF CARBOHYDRATE DERIVATIVES INTO FUNCTIONALIZED CYCLOHEXANES AND CYCLOPENTANES , 1993 .

[34]  N. Chida,et al.  Synthesis of optically active substituted cyclohexenones from carbohydrates by catalytic Ferrier rearrangement , 1991 .

[35]  C. Codina,et al.  Narcissus nivalis: A New Source of Galanthamine1. , 1990, Planta medica.

[36]  M. Miocque,et al.  Analogues morphiniques derives des tetra- et hexahydrodibenzofurannes : I - Synthese et epoxydation stereospecifiques des arylalkylcyclohexenes intermediaires , 1988 .

[37]  R. Webb,et al.  Alkaloid synthesis via intramolecular ene reaction. 2. Application to dl-mesembrine and dl-dihydromaritidine , 1982 .

[38]  J. Luche,et al.  Lanthanoids in organic synthesis. 6. Reduction of .alpha.-enones by sodium borohydride in the presence of lanthanoid chlorides: synthetic and mechanistic aspects , 1981 .

[39]  K. Tomioka,et al.  Stereochemical Studies. LIV. A Biogenetic-type Asymmetric Synthesis of optically Active Galanthamine from L-Tyrosine , 1978 .

[40]  K. Tomioka,et al.  Approaches to the Biogenetic-type Asymmetric Synthesis of Some Amaryllidaceae Alkaloids , 1977 .

[41]  K. Tomioka,et al.  A Biogenetic-type Asymmetric Synthesis of Optically Active Amaryllidaceae Alkaloids: (+)- and (-)-Galanthamine from L-Tyrosine , 1977 .

[42]  Y. Yokoyama,et al.  Phosphorus in organic synthesis—XI Amino acids and peptides—XXI : Reaction of diethyl phosphorocyanidate(DEPC) with carboxylic acids. A new synthesis of carboxylic esters and amides , 1976 .

[43]  T. Shioiri,et al.  Diethylphosphoryl cyanide. A new reagent for the synthesis of amides. , 1973 .

[44]  T. Brocksom,et al.  Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squalene , 1970 .