Ag+ mediated deaminations of N-Boc aryl hydrazines for the efficient synthesis of N-Boc aryl amines

Kang Sang Lee, Young Kwan Lim, Cheon-Gyu Cho

Research output: Contribution to journalArticle

22 Citations (Scopus)

Abstract

N-Boc-aryl hydrazines were converted into N-Boc-aryl amines under the action of Ag+. Its mild reaction conditions tolerate the presence of a variety of functional groups.

Original languageEnglish
Pages (from-to)7463-7464
Number of pages2
JournalTetrahedron Letters
Volume43
Issue number42
DOIs
StatePublished - 2002 Oct 14

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Hydrazines
Deamination
Functional groups
Amines

Cite this

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title = "Ag+ mediated deaminations of N-Boc aryl hydrazines for the efficient synthesis of N-Boc aryl amines",
abstract = "N-Boc-aryl hydrazines were converted into N-Boc-aryl amines under the action of Ag+. Its mild reaction conditions tolerate the presence of a variety of functional groups.",
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Ag+ mediated deaminations of N-Boc aryl hydrazines for the efficient synthesis of N-Boc aryl amines. / Lee, Kang Sang; Lim, Young Kwan; Cho, Cheon-Gyu.

In: Tetrahedron Letters, Vol. 43, No. 42, 14.10.2002, p. 7463-7464.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Ag+ mediated deaminations of N-Boc aryl hydrazines for the efficient synthesis of N-Boc aryl amines

AU - Lee, Kang Sang

AU - Lim, Young Kwan

AU - Cho, Cheon-Gyu

PY - 2002/10/14

Y1 - 2002/10/14

N2 - N-Boc-aryl hydrazines were converted into N-Boc-aryl amines under the action of Ag+. Its mild reaction conditions tolerate the presence of a variety of functional groups.

AB - N-Boc-aryl hydrazines were converted into N-Boc-aryl amines under the action of Ag+. Its mild reaction conditions tolerate the presence of a variety of functional groups.

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JO - Tetrahedron Letters

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