Autor:	Dora Carrico, Sasan Karimi, Sadia Anwar
Rok vydání:	2002
Předmět:	chemistry.chemical_compound chemistry Aldol reaction Bicyclic molecule Tandem Diazomethane Stereochemistry Organic Chemistry Drug Discovery Ring (chemistry) Biochemistry Adduct
Zdroj:	Tetrahedron Letters. 43:33-35
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(01)02072-x
Popis:	Diazomethane ring expansion of 3 followed by deketalization, led to the formation of bicyclodione intermediates 6 and 8. These intermediates underwent internal aldol cyclization to give the tricyclic adducts 7 and 9 in a 1:1 ratio, respectively.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::43b719d45ccfa2721a1900843907031d https://doi.org/10.1016/s0040-4039(01)02072-x Zobrazit plný text záznamu Full Text from ScienceDirect