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 journalArticle

47 Citations (Scopus)

Abstract

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
Volume47
Issue number39
DOIs
StatePublished - Sep 25 2006

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Carbamates
cyclen
succinimide

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

De León-Rodríguez, L. M., Kovacs, Z., Esqueda-Oliva, A. C., & Miranda-Olvera, A. D. (2006). Highly regioselective N-trans symmetrical diprotection of cyclen. Tetrahedron Letters, 47(39), 6937-6940. https://doi.org/10.1016/j.tetlet.2006.07.135

Highly regioselective N-trans symmetrical diprotection of cyclen. / De León-Rodríguez, Luis M.; Kovacs, Zoltan; Esqueda-Oliva, Ana Cristina; Miranda-Olvera, Alma Delia.

In: Tetrahedron Letters, Vol. 47, No. 39, 25.09.2006, p. 6937-6940.

Research output: Contribution to journalArticle

De León-Rodríguez, LM, Kovacs, Z, Esqueda-Oliva, AC & Miranda-Olvera, AD 2006, 'Highly regioselective N-trans symmetrical diprotection of cyclen', Tetrahedron Letters, vol. 47, no. 39, pp. 6937-6940. https://doi.org/10.1016/j.tetlet.2006.07.135
De León-Rodríguez LM, Kovacs Z, Esqueda-Oliva AC, Miranda-Olvera AD. Highly regioselective N-trans symmetrical diprotection of cyclen. Tetrahedron Letters. 2006 Sep 25;47(39):6937-6940. https://doi.org/10.1016/j.tetlet.2006.07.135
De León-Rodríguez, Luis M. ; Kovacs, Zoltan ; Esqueda-Oliva, Ana Cristina ; Miranda-Olvera, Alma Delia. / Highly regioselective N-trans symmetrical diprotection of cyclen. In: Tetrahedron Letters. 2006 ; Vol. 47, No. 39. pp. 6937-6940.
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