Zobrazeno 1 - 4
of 4
pro vyhledávání: '"d-xylofuranose derivatives"'
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 1, Pp 1-8 (2001)
The reactivity of the oxetane ring in 3,5-anhydro-1,2-O-cyclohexylidene- -D-xylofuranose (1) was exemplified by its regiospecific nucleophilic opening. The action of concentrated hydrobromic or hydroiodic acid on 1 resulted in the exclusive formati
Externí odkaz:
https://doaj.org/article/d69d23733d78499a89a63d7d5928a538
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 1, Pp 1-8 (2001)
The reactivity of the oxetane ring in 3,5-anhydro-1,2-O-cyclohexylidene-a-D-xylofuranose (1) was exemplified by its regiospecific nucleophilic opening. The action of concentrated hydrobromic or hydroiodic acid on 1 resulted in the exclusive formation
Externí odkaz:
https://doaj.org/article/7f3d4ffe30e14a019e1f991eff4f4f73
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 1, Pp 1-8 (2001)
The reactivity of the oxetane ring in 3,5-anhydro-1,2-O-cyclohexylidene- -D-xylofuranose (1) was exemplified by its regiospecific nucleophilic opening. The action of concentrated hydrobromic or hydroiodic acid on 1 resulted in the exclusive formation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::068ddd7a4b84f9394192e5b3e1847ca6
https://doi.org/10.2298/jsc0101001h
https://doi.org/10.2298/jsc0101001h
Publikováno v:
Journal of the Serbian Chemical Society, Vol 66, Iss 1, Pp 1-8 (2001)
Scopus-Elsevier
Scopus-Elsevier
The reactivity of the oxetane ring in 3,5-anhydro-1,2-O-cyclohexylidene-a-D-xylofuranose (1) was exemplified by its regiospecific nucleophilic opening. The action of concentrated hydrobromic or hydroiodic acid on 1 resulted in the exclusive formation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::fdde58f8f7e225d43c972a7feba05d05