Highly regioselective N-trans symmetrical diprotection of cyclen

Autor:	Alma D. Miranda-Olvera, Ana Cristina Esqueda-Oliva, Zoltan Kovacs, Luis M. De León-Rodríguez
Rok vydání:	2006
Předmět:	Carbamate chemistry.chemical_compound Cyclen chemistry Succinimide medicine.medical_treatment Organic Chemistry Drug Discovery medicine Organic chemistry Regioselectivity Chloroformate Biochemistry
Zdroj:	Tetrahedron Letters. 47:6937-6940
ISSN:	0040-4039
DOI:	10.1016/j.tetlet.2006.07.135
Popis:	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.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::d46b03163d3d44d3e1580f990d75bb29 https://doi.org/10.1016/j.tetlet.2006.07.135 Zobrazit plný text záznamu Full Text from ScienceDirect