Autor:	Giorgio Molteni, Luisa Garanti
Rok vydání:	2003
Předmět:	Hydrolysis chemistry.chemical_compound Chemistry Organic Chemistry Drug Discovery Organic chemistry Azide Biochemistry
Zdroj:	Tetrahedron Letters. 44:1133-1135
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(02)02844-7
Popis:	The MeOPEG-supported azide 2 was reacted in the presence of a number of alkynyl dipolarophiles. The corresponding 1-MeOPEG-supported-1,2,3-triazoles were obtained in nearly quantitative yields. Acidic hydrolysis of the cycloadducts 5b and 6b caused the removal of the MeOPEG pendant giving 4-methoxycarbonyl-1,2,3-triazole 9 and 5-methoxycarbonyl-1,2,3-triazole 10 , respectively.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::12f4a0475c644e5af62eec8b17034d00 https://doi.org/10.1016/s0040-4039(02)02844-7 Zobrazit plný text záznamu Full Text from ScienceDirect