By an Amadori rearrangement of easily available 5-azido-5-deoxy-D-glucofuranose with dibenzylamine and subsequent catalytic hydrogenation of the resulting 5-azido-l-dibenzylamino-l,5dideoxy-D-fructopyranose, the new l-amino-l,2,5-trideoxy-2,5-ilnino-D-mannitol was obtained in only two steps and exce
β¦ LIBER β¦
Efficient cleavage of terminal acetonide group: Chirospecific synthesis of 2,5-dideoxy-2,5-imino-D-mannitol
β Scribed by Ki Hun Park; Yong Jin Yoon; Sang Gyeong Lee
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 318 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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