By Zbigiew J. Witczak, Kuniaki Tatsuta
Content material: 1. Chiral Carbohydrate development Blocks with a brand new standpoint: Revisited / Zbigniew J. Witczak -- 2. A handy technique for the education of Levoglucosenone and Its Conversion to Novel Chiral Derivatives / Walter S. Trahanovsky, Jason M. Ochaoda, Chen Wang, Kevin D. Revell, Kirk B. Arvidson, Yu Wang, Huiyan Zhao, Steven Chung and Synthia Chang -- three. guidance and Exploitation of an manmade Levoglucosenone / Kunio Ogasawara -- four. Sugar-Derived development Blocks for the Synthesis of Non-Carbohydrate common items / Frieder W. Liechtenthaler -- five. normal 3 Carbon Chiral Synthons from Carbohydrates: Chiral Pool and Chiral Auxiliary ways / Rawle I. Hollingsworth and Guijun Wang
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Additional resources for Carbohydrate Synthons in Natural Products Chemistry. Synthesis, Functionalization, and Applications
We studied the Diels-Alder reaction of levoglucosenone (2) with the very reactive diene 2,3-dimethylene-2,3-dihydrofuran (3), the furan-based or/Ao-quinodimethane, which is readily available by the Flash Vacuum Pyrolysis (FVP) of ester 4. Diene 3 dimerizes very rapidly 9 5 13 810 11-14 15 10 16 16 24 CH -0-£>-Ph flh 2 f< O V^CH fX F W _ ^ -PhCOOH 3 V ^ 4 3 1 * 3 and the thermal reaction of 2 and 3 gave only 12% yield of a mixture of two isomeric cycloadducts, 5 and 6. Addition of the Lewis acid boron trifluoride increased the rate of the Diels-Alder reaction and the yield of products 5 and 6 increased to 40%.
1984, 14, 911-12. ; Horton, D. Cryst. Struct. Commun. 1984, 3, 468-70. ; Essig, M . ; Ward, D. Carbohydr. Res. 1983, 114, 7182. (j) Ward, D. ; Shafizadeh, F. Carbohydr. Res. 1981, 95, 155-76. ; Horton, D. Carbohydr. Res. 1983, 122, 189-99. (a) Isobe, M . ; Nishikawa, T. Front. Biomed. Biotechnol 1992, 2, 99-108. , ref. 5, 99. Miftakhov, M . ; Gaisina, I. ; Valeev, F. A. Ivz. Akad. Nauk. Ser. Khim. 1996, 8, 2047-2049. ; Sauer, V. J. Z. Naturforsch. 1962, 17b, 206. (b) Blake, A. ; Forsyth, A. ; Hewitt, B.
Goto, T. Tetrahedron Lett 1987, 28, 6485-8. (e) Isobe, M . ; Fukami, N . ; Goto, T. Heterocycles 1987, 25, 521-32. (f) Isobe, M . ; Goto, T. Chem. Lett. 1985, 1, 71-4. (g) Ferrier, R. J. J. Chem. Soc, Chem. Commun. 1984, 14, 911-12. ; Horton, D. Cryst. Struct. Commun. 1984, 3, 468-70. ; Essig, M . ; Ward, D. Carbohydr. Res. 1983, 114, 7182. (j) Ward, D. ; Shafizadeh, F. Carbohydr. Res. 1981, 95, 155-76. ; Horton, D. Carbohydr. Res. 1983, 122, 189-99. (a) Isobe, M . ; Nishikawa, T. Front. Biomed.