[1] NUNO M, XAVIER, AMELIA P. Rauter sugars containing α, β-unsaturated carbonyl systems:synthesis and their usefulness as scaffolds in carbohydrate chemistry [J]. Carbohydrate Research 2008, 343. [2] YADAV J S, REDDY B V S, SATHEESH G. InCl3-Catalyzed stereoselective synthesis of 1, 5-benzodiazepines [J]. ARKIVOC 2005. [3] Sagar R, Singh P, Kumar R, Maulik PR, Shaw AK. Diastereoselective annulation of 4-hydroxypyran-2H-ones with enantiopure 2, 3-dideoxy-alpha, beta-unsaturated sugar aldehydes derived from respective glycals [J]. Carbohydrate research 2005, 7(7). [4] YADAV J S, Reddy B V S, PARIMALA G. Bismuth triflate catalyzed condensation of δ-hydroxy-α, β-b-unsaturated aldehydes with aryl amines [J]. Tetrahedron Letters 2004, 45. [5] Jarosz S., Skora S.. A convenient route to enantiomerically pure highly oxygenated decalins from sugar allyltin derivatives [J]. Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry 2000, 6(6). [6] Pathak R., Shaw AK., Bhaduri AP.. Chain extension of acyclic sugar derivatives via the Baylis-Hillman reaction [J]. Tetrahedron 2002, 18(18). [7] Yadav JS, Raju AK, Sunitha V. Highly stereoselective synthesis of C-(alkynyl)-pseudoglycals from delta-hydroxy-alpha, beta-unsaturated aldehydes [J]. Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry 2006, 30(30). [8] Jarosz S, Gawel A. Sugar allyltin compounds: Preparation and application in organic synthesis [J]. European journal of organic chemistry 2005, 16(16). [9] LEVOIRIER E, CANAC Y, NORSIKIAN S. Indium-promoted Barbier-type allylations inaqueous media:aconvenient approach to 4-C-branched monosaccharides and(1→4)-C-disaccharides [J]. Carbohydrate Research 2004, 339. [10] BINKLEY R W. A Mild process for the oxidation of partially protected carbohydrates [J]. Journal of Organic Chemistry 1977, 42. [11] HORTON D, LIAV A. Extension of sugar chains by enolate addition to methyl 2, 3-di-O-acetyl-4-deoxy-β-L-threo-hex-4-enodialdo-1, 5-pyranoside [J]. Carbohydrate Research 1972, 24. [12] MACKIE D M, PERLIN A S. Synthesis of α, β-unsaturated, carbonyl sugar derivatives by methyl sulfoxide oxidetion and elimination [J]. Carbohydrate Research 1972, 24. [13] CREE G M, MACKIE D W, PERLIN A S. Facile elimination accompanying some methyl sulfoxide oxidations:formation of unsaturated carbohydrates [J]. Canadian Journal of Chemistry 1969, 47. [14] BUTTERWORTH R F, HANESSIAN S. Selected methods of oxidation in carbohydrate chemistry [J]. Synthesis 1971. [15] MANCUSO A J, SWERN D. Activated dimethyl sulfoxide:useful reagents for synthesis [J]. Synhesis 1981. [16] LEDERKREMER R M, MARINO C. Acide and other products of oxidation of sugars [J]. Advances in Carbohydrate Chemistry & Biochemistry 2003, 58. [17] HASHIMOTO H, ASANO K, YOSHIMORA J. Synthesis of destomic and epi-destomic acid, and their C-6 epimers [J]. Carbohydrate Research 1982, 104. |