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Tetrahedron. 76(1)
The key step in the syntheses of highly substituted trans-3,4-dihydroxypyrrolidines is introduction of bromide by stereospecific and regiospecific Hanessian-Hullar reactions; benzylidene lactones of l-rhamnonolactone and 6-deoxy-this should be small
The crystalline form of 1-deoxy-o-sorbose, C6H 12O5, is shown to be 1-deoxy-α-D-sorbopyranose. This is the first reported crystal structure of a 1-deoxyketose. The absolute configuration was determined by the use of D-xylose as the starting material
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https://ora.ox.ac.uk/objects/uuid:ae504b33-29b8-4c2b-a60a-f251ade86b4c
https://ora.ox.ac.uk/objects/uuid:ae504b33-29b8-4c2b-a60a-f251ade86b4c
Publikováno v:
ResearcherID
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https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2869d3a8a12860c045140df4c2308d97
https://ora.ox.ac.uk/objects/uuid:64dbf737-3c98-403e-bde4-68c3260f1696
https://ora.ox.ac.uk/objects/uuid:64dbf737-3c98-403e-bde4-68c3260f1696
Title full: 3,6-dideoxy-3,6-imino-1,2-o-isopropylidene-α-d-glucofuranose as a divergent intermediate for the synthesis of hydroxylated pyrrolidines; synthesis of 1,4 dideoxy-1,4-imino-l-gulitol, 1,4-dideoxy-i,4-imino-d-lyxitol, 2S,3S,4R-3,4-dihydrox
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https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::bad7e9b3c99739f15d994c3c016081e7
https://doi.org/10.1016/s0040-4020(01)86851-4
https://doi.org/10.1016/s0040-4020(01)86851-4