Identification of the 2-hydroxymethyl-3,4-dihydroxypyrrolidine (or 1,4-dideoxy-1,4-iminopentitol) from angylocalyx boutiqueanus and from arachniodes standishii as the (2R, 3R, 4S)-isomer by the synthesis of its enantiomer.
โ Scribed by D.Wyn C. Jones; Robert J. Nash; E.Arthur Bell; J.Michael Williams
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 140 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
alkaloid fromAngylocslyxBoutiqueanus. The alkaloid from Arachniodes Standishii,recently reported to have the xylo configuration, was also shown to be the D-arabino isomer.
Naturally occurring hydroxylated piperidine derivatives such as 1,5-dideoxy-1,5-imino-;mannitol' and 1,5-dideoxy-1,5-imino-E-glucitol (deoxynojirimycin)
๐ SIMILAR VOLUMES
## Abstract Pen II [(2__S__,2' __R__,3__R__,3' __E__,4__E__,8__E__)โ1โ__O__โ(ฮฒโDโglucopyranosyl)โ__N__โ(2'โhydroxyโ3'โoctadecenoyl)โ9โmethylโ4,8โsphingadienine], the major component of the cerebrosides isolated from __Penicillium funiculosum__ Aโ1 as the fruiting inducer against __Schizophyllum com