ChemInform Abstract: Synthesis of Indolylquinolines, Indolylacridines, and Indolylcyclopenta[b]quinolines from the Baylis-Hillman Adducts: An in situ [1,3]-Sigmatropic Rearrangement of an Indole Nucleus to Access Indolylacridines and Indolylcyclopenta[b]q

Autor:	Chun Wei Kuo, Ching Fa Yao, Donala Janreddy, Veerababurao Kavala, Chintakunta Ramesh, Po Min Lei
Rok vydání:	2013
Předmět:	Indole test In situ medicine.anatomical_structure Chemistry Stereochemistry Acridine derivatives medicine General Medicine Sigmatropic reaction Nucleus Adduct
Zdroj:	ChemInform. 44
ISSN:	0931-7597
DOI:	10.1002/chin.201305086
Popis:	The coupling of cyclic Baylis—Hillman adducts like (I), (V), and (X) with indoles is found to result in formation of α- or γ-heteroarylated products depending on the nature of educts.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::3f9cab51d97f1f89f6b1ab110993b0cd https://doi.org/10.1002/chin.201305086 Zobrazit plný text záznamu Plný text