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Asymmetric aldol reaction via memory of chirality

โœ Scribed by Watanabe, Hidetoshi; Yoshimura, Tomoyuki; Kawakami, Shimpei; Sasamori, Takahiro; Tokitoh, Norihiro; Kawabata, Takeo


Book ID
120434792
Publisher
Royal Society of Chemistry
Year
2012
Tongue
English
Weight
1015 KB
Volume
48
Category
Article
ISSN
1359-7345

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๐Ÿ“œ SIMILAR VOLUMES


Asymmetric double aldol reaction of chir
โœ Hiroshi Furuno; Tadashi Inoue; Atsushi Abiko ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 135 KB

Treatment of chiral oxazolidinone with Bu 2 BOTf (2.5 equiv.) and Et 3 N (3.0 equiv.) quantitatively produced the doubly borylated enolate, which afforded the double aldol products with high diastereoselectivity after reaction with aldehydes.