Asymmetric control in the Pictet-Spengler reaction by means of N-protected amino acids as chiral auxiliary groups

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Institut für Organische Chemie, Universität Karlsruhe, Richard-Willstätter-Allee 2, D-76128 Karlsruhe, Germany ^{[1
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Chem. Eur. J. | / 12卷 / 1566-1571期

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[43] General approach for the synthesis of macroline/sarpagine related indole alkaloids via the asymmetric Pictet-Spengler reaction: The enantiospecific synthesis of the N-a-H, azabicyclo[3.3.1]nonone template
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[48] Chiral oxime ethers in asymmetric synthesis.: Part 4.: Asymmetric synthesis of N-protected amines and β-amino acids by the addition of organometallic reagents to ROPHy/SOPHy-derived aldoximes
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[50] A rapid and efficient one-pot method for the reduction of N-protected α-amino acids to chiral α-amino aldehydes using CDI/DIBAL-H
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