Highly regioselective N-trans symmetrical diprotection of cyclen

Luis M. De León-Rodríguez, Zoltan Kovacs, Ana Cristina Esqueda-Oliva, Alma Delia Miranda-Olvera

Research output: Contribution to journalArticlepeer-review

55 Scopus citations


A high yielding N-trans diprotection procedure for cyclen has been developed by using succinimide carbamate derivates of Boc and Cbz and chloroformate protecting groups.

Original languageEnglish (US)
Pages (from-to)6937-6940
Number of pages4
JournalTetrahedron Letters
Issue number39
StatePublished - Sep 25 2006

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry


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