Novel applications of resin bound α-amino acids for the synthesis of benzodiazepines (via Wang resin) and ketopiperazines (via hydroxymethyl resin)

  • Christopher Hulme
  • , Liang Ma
  • , N. Vasant Kumar
  • , Paul H. Krolikowski
  • , Andrew C. Allen
  • , Richard Labaudiniere

Research output: Contribution to journalArticlepeer-review

66 Scopus citations

Abstract

This communication reveals a novel application of resin bound α-amino acids coupled with the UDC (Ugi/DeBOC/cyclize) strategy. Reaction with either N-BOC-α-amino aldehydes or N-BOC anthranilic acids and subsequent acid treatment allows the preparation of highly pure and diverse arrays (approx. 10000 in size) of 1,4-benzodiazepines (Wang resin) and ketopiperazines (hydroxymethyl resin), respectively. Notable for the benzodiazepine series of compounds are the five potential points of diversity available from this two-step protocol.

Original languageEnglish (US)
Pages (from-to)1509-1514
Number of pages6
JournalTetrahedron Letters
Volume41
Issue number10
DOIs
StatePublished - Mar 4 2000
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Fingerprint

Dive into the research topics of 'Novel applications of resin bound α-amino acids for the synthesis of benzodiazepines (via Wang resin) and ketopiperazines (via hydroxymethyl resin)'. Together they form a unique fingerprint.

Cite this