Lactonisation and lactone ether formation of nerol geraniol compounds. Use of 13C to identify the cyclisation process

[1]  C. Lavaud,et al.  New method for the determination of the absolute stereochemistry in antitumoral annonaceous acetogenins , 1998 .

[2]  H. Koshino,et al.  STEREOSELECTIVE SYNTHESIS OF TETRAHYDROPYRAN AND OXEPANE SYSTEMS BY THE ENDO-CYCLIZATION OF HYDROXY STYRYLEPOXIDES , 1997 .

[3]  F. McDonald,et al.  syn-Oxidative Polycyclizations of Hydroxypolyenes: Highly Stereoselective and Potentially Biomimetic Syntheses of all-trans-Polytetrahydrofurans , 1997 .

[4]  K. Nacro,et al.  Stereoselective synthesis of five and/or six membered ring hydroxylactones obtained by Lewis acid mediated reaction of γ,δ-epoxy-β-hydroxyesters; access to 5-methylated 2-deoxysugars. , 1997 .

[5]  K. Nacro,et al.  Enhanced diastereoselectivity in the addition of ester enolate to optically active α,β-epoxyaldehydes obtained from nerol and geraniol , 1996 .

[6]  J. Hartung,et al.  Ring Closure Reactions of Substituted 4-Pentenyl-1-oxy Radicals. The Stereoselective Synthesis of Functionalized Disubstituted Tetrahydrofurans , 1995 .

[7]  E. Álvarez,et al.  Useful Designs in the Synthesis of trans-Fused Polyether Toxins , 1995 .

[8]  L. Paquette,et al.  OXONIUM ION-INITIATED PINACOLIC RING EXPANSION REACTIONS. APPLICATION TO THE ENANTIOSELECTIVE SYNTHESIS OF THE SPIROCYCLIC SESQUITERPENE ETHERS DACTYL OXENE-B AND -C , 1995 .

[9]  J. Harmange,et al.  Synthetic routes to 2,5-disubstituted tetrahydrofurans , 1993 .

[10]  M. Baltas,et al.  Diastereoface differentiation in addition of lithium enolates to chiral α,β-epoxyaldehydes , 1993 .

[11]  S. Mclean,et al.  Quassiol A, a novel squalene triterpene from , 1993 .

[12]  M. Baltas,et al.  A short synthesis of substituted β-hydroxy γ-butyrolactones and 2-deoxyhexofuranosides , 1992 .

[13]  G. Cardillo,et al.  Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediates , 1990 .

[14]  T. Kan,et al.  Total syntheses of (+)-thyrsiferol, (+)-thyrsiferyl 23-acetate, and (+)-venustatriol , 1990 .

[15]  S. Reich,et al.  Enantioselective total synthesis of 9S-dihydroerythronolide A seco acid , 1989 .

[16]  K. Nicolaou,et al.  Activation of 6-endo over 5-exo hydroxy epoxide openings. Stereoselective and ring selective synthesis of tetrahydrofuran and tetrahydropyran systems , 1989 .

[17]  E. Corey,et al.  The Logic of Chemical Synthesis , 1989 .

[18]  Taryn L. B. Boivin Synthetic routes to tetrahydrofuran, tetrahydropyran, and spiroketal units of polyether antibiotics and a survey of spiroketals of other natural products , 1987 .

[19]  L. Jaenicke Ionophore Polyether Antibiotics – Naturally Occurring Acid Ionophores. Bd. 1: Biology. Von J. W. Westley. Marcel Dekker, Inc., New York – Basel 1982. XVII, 465 S., SFr. 185,– , 1983 .

[20]  J. Baldwin,et al.  Rules for ring closure: ring formation by conjugate addition of oxygen nucleophiles , 1977 .

[21]  W. Herz,et al.  Ligantrol and ligantrol monoacetate, two new linear polyoxygenated Diterpenes from Liatris elegans , 1975 .