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Stereospecific synthesis of 5,6-dihydro-2H-pyran system. High-pressure cycloaddition of 1:2,3:4-di-0-isopropylidene- α-D-galactopyranose-6-ulose to 1-methoxybuta-1,3-diene

✍ Scribed by Janusz Jurczak; Tomasz Bauer; Sławomir Jarosz


Book ID
104233891
Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
237 KB
Volume
25
Category
Article
ISSN
0040-4039

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✦ Synopsis


The high-pressure cycloaddition of 1:2,3:4-di-0-isopropyIidene-0(*2-galactopyra-) . It is noteworthy that the specific rotation of diastereoisomer 2 with opposite configuration at c-6 was [MID-81°(cl,CHC13). w


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✍ Usama A.R. Al-Timari; L̆ubor Fis̆era; Igor Goljer; Peter Ertl 📂 Article 📅 1992 🏛 Elsevier Science 🌐 English ⚖ 540 KB

The synthesis of 2-phenyl-3-aryl and 2-phenyl-3-aroyl derivatives 5-(1,2-O-isopropylidene-alpha-D-xylo-tetrofuranos-4-yl)isoxazolidi ne (3) from nitrones and 5,6-dideoxy-1,2-O-isopropylidene-alpha-D-xylo-hex-5- enofuranose (1) is described. The 1,3-dipolar cycloaddition reactions given mainly anti a