Highly regioselective N-trans symmetrical diprotection of cyclen

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

doi:10.1016/j.tetlet.2006.07.135

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 journal › Article › peer-review

56 Scopus citations

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 language	English (US)
Pages (from-to)	6937-6940
Number of pages	4
Journal	Tetrahedron Letters
Volume	47
Issue number	39
DOIs	https://doi.org/10.1016/j.tetlet.2006.07.135
State	Published - Sep 25 2006

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2006.07.135

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title = "Highly regioselective N-trans symmetrical diprotection of cyclen",

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.",

author = "{De Le{\'o}n-Rodr{\'i}guez}, {Luis M.} and Zoltan Kovacs and Esqueda-Oliva, {Ana Cristina} and Miranda-Olvera, {Alma Delia}",

note = "Funding Information: Supported by grants from CONCYTEG GTO-2002-C01-6029 and GTO-2003-C02-11517.",

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AU - De León-Rodríguez, Luis M.

AU - Kovacs, Zoltan

AU - Esqueda-Oliva, Ana Cristina

AU - Miranda-Olvera, Alma Delia

N1 - Funding Information: Supported by grants from CONCYTEG GTO-2002-C01-6029 and GTO-2003-C02-11517.

PY - 2006/9/25

Y1 - 2006/9/25

N2 - 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.

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M3 - Article

AN - SCOPUS:33747769692

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JO - Tetrahedron Letters

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ER -

Highly regioselective N-trans symmetrical diprotection of cyclen

Abstract

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