Convenient synthesis of [3]catenane by olefin metathesis dimerizations

Autor:	Hiroyuki Nagamiya, Yoshimasa Fukazawa, Hajime Iwamoto, Koji Itoh
Rok vydání:	2003
Předmět:	Ring size Ring-closing metathesis Olefin metathesis Chemistry Organic Chemistry Drug Discovery Catenane Polymer chemistry Organic chemistry Ring-opening metathesis polymerisation Biochemistry Acyclic diene metathesis
Zdroj:	Tetrahedron Letters. 44:5773-5776
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(03)01424-2
Popis:	[3]Catenane 5a and 5b were synthesized conveniently by olefin metathesis dimerization of pseudorotaxanes 3a and 3b . The yields of 5a and 5b were influenced by concentrations of 3a and 3b , and a ring size of a center wheel of [3]catenane.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::38df4e1ef48564f084356741fe657f4c https://doi.org/10.1016/s0040-4039(03)01424-2 Zobrazit plný text záznamu Full Text from ScienceDirect