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Nucleophilic cleavage of acetals using organometallic reagents

✍ Scribed by Atsunori Mori; Junya Fujiwara; Keiji Maruoka; Hisashi Yamamoto

Book ID
103224320
Publisher
Elsevier Science
Year
1985
Tongue
English
Weight
869 KB
Volume
285
Category
Article
ISSN
0022-328X

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πŸ“œ SIMILAR VOLUMES

Asymmetric reduction of ketone reductive
Asymmetric reduction of ketone reductive cleavage of chiral acetals using organoaluminum reagents
✍ Atsunori Mori; Junya Fujiwara; Keiji Maruoka; Hisashi Yamamoto πŸ“‚ Article πŸ“… 1983 πŸ› Elsevier Science 🌐 French βš– 229 KB

Some chiral acetals are cleaved by organoaluminum reagents. The products are formed diastereoselectively, and the removal of the chiral auxiliary affords optically active alcohols. A recent communication by Bartlett, Johnson and Elliott1 on the acetal derived from (-)-(2$4\_R)-2,4-pentanediol has pr