Nucleophilic opening of the oxetane rings in 3,5-anhydro-1,2,O-isopropylidene-.beta.-L-idofuranose and .alpha.-D-xylofuranose
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo01265a080
Cited by 22 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. The Construction of Anhydro Monosaccharides;Asian Journal of Organic Chemistry;2016-10-25
2. Formation of Substituted Tetrahydropyrans through Oxetane Ring Opening: Application to the Synthesis of C1–C17 Fragment of Salinomycin;Organic Letters;2014-01-30
3. Acid promoted intramolecular formation of 3,5-anhydro-1,4-furano-7-ulose derivatives via the Wittig-cyclization procedure and their antimicrobial properties;Medicinal Chemistry Research;2012-09-18
4. Synthesis and biological evaluation of deoxy salacinols, the role of polar substituents in the side chain on the α-glucosidase inhibitory activity;Bioorganic & Medicinal Chemistry;2006-01
5. Hydroxy group interactions in stannylated carbohydrates. Structures and thermal stabilities of 5-deoxy-5-C-(Ph3Sn)-1,2-O-isopropylidene-α-D-xylofuranose, 5-deoxy-5-C-(IPh2Sn)-1,2-O-isopropylidene-α-D- and -L-xylofuranose, and 5-deoxy-5-C-(I2PhSn)-1,2-O-isopropylidene-α-D- and -L-xylofuranose;J. Chem. Soc., Perkin Trans. 1;2002
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