A total synthesis of the natural enantiomer of the title compound was accomplished, which confirmed the structure proposed for the fruitinginducing cerebroside of Schizophyllum commune. Fruiting body formation in Basidiomycetes is indeed a spectacular phenomenon especially to those who love to taste
✦ LIBER ✦
Synthesis of (4E,8E,2S,3R,2'R)-N-2' -hydroxyhexadecanoyl-9-methyl-4,8-sphingadiemine, the ceramide portion of the fruiting-inducing cerebroside in a basidiomycete schizophyllum commune, and its (2R,3S)-isomer
✍ Scribed by Kenji Mori; Yuji Funaki
- Book ID
- 108374442
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 941 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4020
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## Abstract Pen II [(2__S__,2' __R__,3__R__,3' __E__,4__E__,8__E__)‐1‐__O__‐(β‐D‐glucopyranosyl)‐__N__‐(2'‐hydroxy‐3'‐octadecenoyl)‐9‐methyl‐4,8‐sphingadienine], the major component of the cerebrosides isolated from __Penicillium funiculosum__ A‐1 as the fruiting inducer against __Schizophyllum com
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