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Stereoselective aldol reaction of glutarimides using pseudo C(2) symmetry.

Organic letters (2009-12-22)
Yohsuke Watanabe, Takashi Yamazaki, Toshio Kubota
ABSTRACT

The boron aldol reaction of beta-substituted glutaric imides bearing an oxazolidinone-based auxiliary proceeds with excellent diastereoselectivity; switching the tertiary amine employed between i-Pr(2)EtN or Et(3)N affords enantiomeric lactone product.

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Sigma-Aldrich
Glutarimide, 98%