Lewis acid-induced rearrangement of the Diels–Alder dimer of tetrachlorocyclopentadienone: structure reassignments

Autor:	Richard Gilardi, Philip E. Eaton, Datong Tang
Rok vydání:	2002
Předmět:	chemistry.chemical_compound Chemistry Stereochemistry Dimer Organic Chemistry Drug Discovery Diels alder Lewis acids and bases Biochemistry Isomerization
Zdroj:	Tetrahedron Letters. 43:3-5
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(01)02085-8
Popis:	The structures of various perhalodiones available by isomerization of the Diels–Alder dimers of tetrachloro- and tetrabromocyclopentadienone have finally been determined unambiguously.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::5f08cbaf5acdaee47fc5edb0c19c32ef https://doi.org/10.1016/s0040-4039(01)02085-8 Zobrazit plný text záznamu Full Text from ScienceDirect