An effective conversion of N'-ethoxymethylene-2-(N-bocamino) propionohydrazides into 2-(1-aminoethyl)-1,3,4-oxadiazoles

Agnieszka Kudelko; Wojciech Zieliński

doi:10.3998/ark.5550190.0010.e01

An effective conversion of N'-ethoxymethylene-2-(N-bocamino) propionohydrazides into 2-(1-aminoethyl)-1,3,4-oxadiazoles

Agnieszka Kudelko
, Wojciech Zieliński

Katedra Technologii Chemicznej Organicznej i Petrochemii (RCH/RCH5)

Silesian University of Technology

Wyniki badań: Wkład do czasopisma › Artykuł › recenzja

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Abstrakt

A series of N'-ethoxymethylene-2-(N-Boc-amino)propionohydrazide derivatives was obtained from the reactions of N-Boc-protected alanine hydrazide and triethyl orthoesters. They underwent cyclization to the corresponding 2-(1-N-Boc-aminoethyl)-1,3,4-oxadiazoles in glacial acetic acid.

Język oryginału	angielski
Strony (od–do)	1-8
Liczba stron	8
Czasopismo	Arkivoc
Tom	2009
Numer wydania	14
Identyfikatory DOI	https://doi.org/10.3998/ark.5550190.0010.e01
Status publikacji	Opublikowano - 2009

Obszary tematyczne ASJC Scopus

Chemia organiczna

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10.3998/ark.5550190.0010.e01

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title = "An effective conversion of N'-ethoxymethylene-2-(N-bocamino) propionohydrazides into 2-(1-aminoethyl)-1,3,4-oxadiazoles",

abstract = "A series of N'-ethoxymethylene-2-(N-Boc-amino)propionohydrazide derivatives was obtained from the reactions of N-Boc-protected alanine hydrazide and triethyl orthoesters. They underwent cyclization to the corresponding 2-(1-N-Boc-aminoethyl)-1,3,4-oxadiazoles in glacial acetic acid.",

keywords = "Boc protecting group, Cyclization, N'-ethoxymethylene-2-(N-Boc-amino)propionohydrazide, 1,3,4-Oxadiazole, Syn and anti isomerism",

author = "Agnieszka Kudelko and Wojciech Zieli{\'n}ski",

year = "2009",

doi = "10.3998/ark.5550190.0010.e01",

language = "English",

volume = "2009",

pages = "1--8",

journal = "Arkivoc",

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T1 - An effective conversion of N'-ethoxymethylene-2-(N-bocamino) propionohydrazides into 2-(1-aminoethyl)-1,3,4-oxadiazoles

AU - Kudelko, Agnieszka

AU - Zieliński, Wojciech

PY - 2009

Y1 - 2009

N2 - A series of N'-ethoxymethylene-2-(N-Boc-amino)propionohydrazide derivatives was obtained from the reactions of N-Boc-protected alanine hydrazide and triethyl orthoesters. They underwent cyclization to the corresponding 2-(1-N-Boc-aminoethyl)-1,3,4-oxadiazoles in glacial acetic acid.

AB - A series of N'-ethoxymethylene-2-(N-Boc-amino)propionohydrazide derivatives was obtained from the reactions of N-Boc-protected alanine hydrazide and triethyl orthoesters. They underwent cyclization to the corresponding 2-(1-N-Boc-aminoethyl)-1,3,4-oxadiazoles in glacial acetic acid.

KW - Boc protecting group

KW - Cyclization

KW - N'-ethoxymethylene-2-(N-Boc-amino)propionohydrazide, 1,3,4-Oxadiazole

KW - Syn and anti isomerism

UR - https://www.scopus.com/pages/publications/77953194251

U2 - 10.3998/ark.5550190.0010.e01

DO - 10.3998/ark.5550190.0010.e01

M3 - Article

AN - SCOPUS:77953194251

SN - 1551-7004

VL - 2009

SP - 1

EP - 8

JO - Arkivoc

JF - Arkivoc

IS - 14

ER -

An effective conversion of N'-ethoxymethylene-2-(N-bocamino) propionohydrazides into 2-(1-aminoethyl)-1,3,4-oxadiazoles

Abstrakt

Obszary tematyczne ASJC Scopus

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