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ChemInform Abstract: Enolic Orthoesters. Part 6. A New 'Pyranose→Cyclohexane' Transformation via 1,6-Dideoxy-1,1-ethylenedioxy-2,3,4-tri-O-methyl-D- xylo-hex-5-enopyranose

Autor: AI Hibberd, M. D. Mcleod, David J. Collins, D. G. Bourke

Publikováno v: ChemInform. 27

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7c8866d5e4d1e762c5574aa2af4f98fa
https://doi.org/10.1002/chin.199635216

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Enolic Ortho Esters. VI. A New 'Pyranose→Cyclohexane' Transformation via 1,6-Dideoxy-1,1-ethylenedioxy-2,3,4-tri-O-methyl-D-xylo-hex-5-enopyranose

Autor: David J. Collins, D. G. Bourke, AI Hibberd, Mcleod

Publikováno v: Australian Journal of Chemistry. 49:425

Hydrolysis of methyl 6-chloro-6-deoxy-2,3,4-tri-O-methyl-α-D-glucopyranoside (19b) and Swern oxidation of the resulting anomeric hemiacetals (20) gave 6-chloro-6-deoxy-2,3,4-tri-O-methyl-D-glucono-1,5-lactone (21), treatment of which with 1,2-bis( t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6d5c7ce05e4e3f7b7056338f3c5ba259
https://doi.org/10.1071/ch9960425

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c. Enolic Ortho Esters. VI. A New 'Pyranose→Cyclohexane' Transformation via 1,6-Dideoxy-1,1-ethylenedioxy-2,3,4-tri-O-methyl-D-xylo-hex-5-enopyranose (Vol 49, Pg 425, 1996)

Autor: David J. Collins, D. G. Bourke, AI Hibberd, Mcleod

Publikováno v: Australian Journal of Chemistry. 49:646

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a2b18acbc635eefb87a29006f0e3753b
https://doi.org/10.1071/ch9960646ac

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