Synthesis of 1,7-dioxaspiro[5.5]undecanes and 1-oxa-7-thiaspiro[5.5]undecanes from exo-glycal
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[1] R. Hartley,et al. Synthesis of spiroacetals using functionalised titanium carbenoids , 2008 .
[2] Chun-Hung Lin,et al. Different reaction routes found in acid-catalyzed glycosylation of endo- and exo-glycals: competition between Ferrier rearrangement and protonation , 2005 .
[3] G. O'Doherty,et al. De novo synthesis of a galacto-papulacandin moiety via an iterative dihydroxylation strategy , 2005 .
[4] H. Overkleeft,et al. Synthesis and elaboration of functionalised carbohydrate-derived spiroketals. , 2004, Organic & biomolecular chemistry.
[5] Chung-Yi Wu,et al. Stereoselective glycosylation of exo-glycals accelerated by Ferrier-type rearrangement. , 2003, Organic Letters.
[6] Chuan-Fa Chang,et al. Inter- and intramolecular alcohol additions to exo-glycals , 2002 .
[7] F. K. Griffin,et al. A Ramberg−Bäcklund Approach to the Synthesis ofC-Glycosides,C-Linked Disaccharides, andC-Glycosyl Amino Acids , 2002 .
[8] G. O'Doherty,et al. Enantioselective synthesis of the papulacandin ring system: conversion of the mannose diastereoisomer into a glucose stereoisomer. , 2000, Organic letters.
[9] T. Prangé,et al. Rearrangement of spiroacetals of the 1,6-Dioxaspiro[4.5]decan-10-yl methanesulfonate type. Synthesis of cis-fused 1,6-dioxadecalins. , 2000, The Journal of organic chemistry.
[10] M. Alcaraz,et al. SYNTHETIC APPLICATIONS OF RAMBERG-BACKLUND DERIVED EXO-GLYCALS , 1998 .
[11] H. Overkleeft,et al. A novel and flexible synthesis of pyranose spiroacetal derivatives , 1998 .
[12] E. Suárez,et al. Synthesis of Chiral Spiroacetals from Carbohydrates. , 1995, The Journal of organic chemistry.
[13] N. Kari,et al. Synthesis of a mixture of (2S,5R)- and (2S,5S)-2-methyl-1,6-dioxaspiro[4.5]decane, the odor bouquet minor components of Paravespula vulgaris (L.), from l-sorbose , 1995 .
[14] Davidr . Evans,et al. Total Synthesis of the Polyether Antibiotic Lonomycin A (Emericid) , 1995 .
[15] N. Kari,et al. Synthesis of optically active chalcogran from l-sorbose , 1994 .
[16] M. Rizzacasa,et al. Convergent synthesis of polyether ionophore antibiotics: protective manipulation and synthesis of monensin A , 1993 .
[17] J. Armstrong,et al. Convergent synthesis of polyether ionophore antibiotics: Synthesis of the spiroketal and tricyclic glycal segments of monensin , 1993 .
[18] A. C. Richardson,et al. Enantiospecific synthesis of (R)-1,6-dioxaspiro[4.5]decane from a derivative of d-fructose , 1993 .
[19] R. Schmidt,et al. Spiroketal Synthesis. — A Case of Intramolecular Glycoside Bond Formation , 1992 .
[20] Y. Leblanc,et al. Synthesis of 2-amino C-glucosides and 2-amino C-glucosides spiroketals , 1991 .
[21] R. H. Green,et al. Avermectins and milbemycins Part I , 1991 .
[22] Françoise Perron,et al. Chemistry of spiroketals , 1989 .
[23] M. Brimble,et al. Chemistry of bis-spiroacetals. Synthesis of the 1,6,8-trioxadispiro[4.1.5.3]pentadecane ring system , 1988 .
[24] 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 .
[25] G. Schulte,et al. Model studies directed toward the avermectins: A route to the spiroketal subunit , 1987 .
[26] A. Kluge. Synthesis of 1,7-Dioxaspiro[5.5]undecanes , 1986 .
[27] I. Kay,et al. Spiroketals: a total synthesis of (±)-talaromycin B via a stereoselective cation-olefin cyclisation step , 1984 .
[28] 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 .
[29] G. Remy,et al. Synthèses et epimérisation de déoxy-spiro C-1 sucres , 1983 .
[30] I. Kay,et al. Spiroketals: The synthesis of an olive fly pheromone component, 4-hydroxy-1,7-dioxaspiro[5,5]undecane, via a novle cation-olefin cyclisation step , 1983 .
[31] P. Howse,et al. Identification and synthesis of the major sex pheromone of the olive fly (Dacus oleae) , 1980 .
[32] J. Apsimon. The Total Synthesis of Natural Products , 1973 .