Concise, stereocontrolled synthesis of the citrinadin B core architecture.

Carlos A Guerrero, Erik J Sorensen
Author Information
  1. Carlos A Guerrero: Frick Laboratory, Department of Chemistry, Princeton University, Princeton, New Jersey 08544, USA.

Abstract

A concise, stereocontrolled synthesis of the citrinadin B core architecture from scalemic, readily available starting materials is disclosed. Highlights include ready access to both cyclic tryptophan tautomer and trans-2,6-disubstituted piperidine fragments, an efficient, stereoretentive mixed Claisen acylation for the coupling of these halves, and further diastereoselective carbonyl addition and oxidative rearrangement for assembly of the core.

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Grants

  1. F32 GM086035/NIGMS NIH HHS
  2. R01-GM065483/NIGMS NIH HHS
  3. R01 GM065483-09/NIGMS NIH HHS
  4. F32-GM086035/NIGMS NIH HHS
  5. R01 GM065483/NIGMS NIH HHS

MeSH Term

Esters
Indole Alkaloids
Molecular Structure
Stereoisomerism

Chemicals

Esters
Indole Alkaloids
citrinadin A

Word Cloud

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