Matches in SemOpenAlex for { <https://semopenalex.org/work/W2143668306> ?p ?o ?g. }
- W2143668306 endingPage "3948" @default.
- W2143668306 startingPage "3948" @default.
- W2143668306 abstract "A variety of alcohols react with 2,3,4,6-tetra-O-acetyl-1,5-anhydro-D-arabino-hex-1-enopyranose 1 in the presence of a catalytic amount of HClO(4) supported on silica gel to give the corresponding alkyl 3-deoxy-hex-2-enopyranosides 2 in high yield, with short reaction times (10-45 mins) and good alpha-selectivity. Work-up merely involves filtration of the reagent, followed by chromatographic purification of the crude product. This methodology has also been employed in the synthesis of a bicyclic ether, a useful precursor for cyclic polyethers, and a 4-amino-C-glucoside." @default.
- W2143668306 created "2016-06-24" @default.
- W2143668306 creator A5059311354 @default.
- W2143668306 creator A5064092175 @default.
- W2143668306 creator A5067642249 @default.
- W2143668306 creator A5077552707 @default.
- W2143668306 date "2008-01-01" @default.
- W2143668306 modified "2023-09-24" @default.
- W2143668306 title "HClO4·SiO2 catalysed synthesis of alkyl 3-deoxy-hex-2-enopyranosides from 2-hydroxy glucal ester: application in the synthesis of a cis-fused bicyclic ether and a 4-amino-C-glucoside" @default.
- W2143668306 cites W1968922315 @default.
- W2143668306 cites W1972163887 @default.
- W2143668306 cites W1973213040 @default.
- W2143668306 cites W1976894600 @default.
- W2143668306 cites W1977017667 @default.
- W2143668306 cites W1980397054 @default.
- W2143668306 cites W1980500394 @default.
- W2143668306 cites W1982457435 @default.
- W2143668306 cites W1982872101 @default.
- W2143668306 cites W1983953260 @default.
- W2143668306 cites W1986423907 @default.
- W2143668306 cites W1988209223 @default.
- W2143668306 cites W1990676594 @default.
- W2143668306 cites W1992288213 @default.
- W2143668306 cites W1994478313 @default.
- W2143668306 cites W1997352368 @default.
- W2143668306 cites W2003110548 @default.
- W2143668306 cites W2006621472 @default.
- W2143668306 cites W2008436417 @default.
- W2143668306 cites W2017260680 @default.
- W2143668306 cites W2021210793 @default.
- W2143668306 cites W2022362394 @default.
- W2143668306 cites W2023661030 @default.
- W2143668306 cites W2026715465 @default.
- W2143668306 cites W2028169707 @default.
- W2143668306 cites W2034605479 @default.
- W2143668306 cites W2034779160 @default.
- W2143668306 cites W2038017418 @default.
- W2143668306 cites W2039326874 @default.
- W2143668306 cites W2041823821 @default.
- W2143668306 cites W2042760452 @default.
- W2143668306 cites W2048579489 @default.
- W2143668306 cites W2049017871 @default.
- W2143668306 cites W2059760023 @default.
- W2143668306 cites W2061185424 @default.
- W2143668306 cites W2062500776 @default.
- W2143668306 cites W2063205686 @default.
- W2143668306 cites W2076492888 @default.
- W2143668306 cites W2083826336 @default.
- W2143668306 cites W2090013104 @default.
- W2143668306 cites W2090319365 @default.
- W2143668306 cites W2091868550 @default.
- W2143668306 cites W2116741024 @default.
- W2143668306 cites W2132097259 @default.
- W2143668306 cites W2140897818 @default.
- W2143668306 cites W2149511774 @default.
- W2143668306 cites W2156844402 @default.
- W2143668306 cites W2162971359 @default.
- W2143668306 cites W2168474959 @default.
- W2143668306 cites W2174778255 @default.
- W2143668306 cites W2176099791 @default.
- W2143668306 cites W2177850328 @default.
- W2143668306 cites W2178313176 @default.
- W2143668306 cites W2178560928 @default.
- W2143668306 cites W2332332221 @default.
- W2143668306 cites W2553731662 @default.
- W2143668306 cites W2949524193 @default.
- W2143668306 cites W2949766254 @default.
- W2143668306 cites W2950667118 @default.
- W2143668306 cites W2951913279 @default.
- W2143668306 cites W2952107618 @default.
- W2143668306 cites W2952109280 @default.
- W2143668306 cites W2952612467 @default.
- W2143668306 cites W2953307993 @default.
- W2143668306 cites W4233211793 @default.
- W2143668306 cites W4246338188 @default.
- W2143668306 doi "https://doi.org/10.1039/b810654a" @default.
- W2143668306 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/18931801" @default.
- W2143668306 hasPublicationYear "2008" @default.
- W2143668306 type Work @default.
- W2143668306 sameAs 2143668306 @default.
- W2143668306 citedByCount "18" @default.
- W2143668306 countsByYear W21436683062012 @default.
- W2143668306 countsByYear W21436683062013 @default.
- W2143668306 countsByYear W21436683062014 @default.
- W2143668306 countsByYear W21436683062016 @default.
- W2143668306 countsByYear W21436683062017 @default.
- W2143668306 countsByYear W21436683062018 @default.
- W2143668306 countsByYear W21436683062019 @default.
- W2143668306 countsByYear W21436683062020 @default.
- W2143668306 countsByYear W21436683062021 @default.
- W2143668306 countsByYear W21436683062022 @default.
- W2143668306 crossrefType "journal-article" @default.
- W2143668306 hasAuthorship W2143668306A5059311354 @default.
- W2143668306 hasAuthorship W2143668306A5064092175 @default.
- W2143668306 hasAuthorship W2143668306A5067642249 @default.
- W2143668306 hasAuthorship W2143668306A5077552707 @default.
- W2143668306 hasConcept C118792377 @default.
- W2143668306 hasConcept C134121241 @default.