Organic letters

Progress toward the total synthesis of callipeltin A (I): asymmetric synthesis of (3 S, 4 R)-3, 4-dimethylglutamine

B Liang, PJ Carroll, MM Joullié

Index: Liang, Bo; Carroll, Patrick J.; Joullie, Madeleine M. Organic Letters, 2000 , vol. 2, # 26 p. 4157 - 4160

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Citation Number: 56

Abstract

During the total synthesis of the novel cyclic depsipeptide callipeltin A (1), the unit (3 S, 4 R)- 3, 4-dimethylglutamine, was successfully synthesized by asymmetric Michael addition and subsequent electrophilic azidation. The key feature of this approach is the generation of three adjacent stereogenic centers using the same camphorsultam chiral auxiliary.

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