IBS Publications Repository: Direct diversification of unmasked quinazolin-4(3H)-ones through orthogonal reactivity modulation

BROWSE

Related Scientist

myung,kyungjae's photo.

myung,kyungjae: 유전체항상성연구단

ITEM VIEW & DOWNLOAD

IBS Publications RepositoryCenter for Genomic Integrity(유전체 항상성 연구단)1. Journal Papers (저널논문)

Direct diversification of unmasked quinazolin-4(3H)-ones through orthogonal reactivity modulation

DC Field	Value	Language
dc.contributor.author	Jae Bin Lee	-
dc.contributor.author	Mi Eun Kang	-
dc.contributor.author	Joohee Kim	-
dc.contributor.author	Chang Young Lee	-
dc.contributor.author	Jung-Min Kee	-
dc.contributor.author	Kyungjae Myung	-
dc.contributor.author	Jang-Ung Park	-
dc.contributor.author	Sung You Hong	-
dc.date.available	2018-01-08T05:16:44Z	-
dc.date.created	2017-10-19	-
dc.date.issued	2017-09	-
dc.identifier.issn	1359-7345	-
dc.identifier.uri	https://pr.ibs.re.kr/handle/8788114/4173	-
dc.description.abstract	Here we report a set of direct functionalization methods of unmasked 2-phenylquinazolin-4(3H)-ones, a privileged alkaloid core, without the installation/removal event of protecting groups or exogenous coordinating moieties. Divergent pathways were modulated with transition-metal catalysts by suppressing competitive reactivities, leading to N-arylation, annulative pi-extension, or C-H fluorination. This journal is © The Royal Society of Chemistry 2017	-
dc.description.uri	1	-
dc.language	영어	-
dc.publisher	ROYAL SOC CHEMISTRY	-
dc.title	Direct diversification of unmasked quinazolin-4(3H)-ones through orthogonal reactivity modulation	-
dc.type	Article	-
dc.type.rims	ART	-
dc.identifier.wosid	000411187100011	-
dc.identifier.scopusid	2-s2.0-85029612981	-
dc.identifier.rimsid	60565	ko
dc.date.tcdate	2018-10-01	-
dc.contributor.affiliatedAuthor	Kyungjae Myung	-
dc.contributor.affiliatedAuthor	Sung You Hong	-
dc.identifier.doi	10.1039/c7cc05794f	-
dc.identifier.bibliographicCitation	CHEMICAL COMMUNICATIONS, v.53, no.75, pp.10394 - 10397	-
dc.citation.title	CHEMICAL COMMUNICATIONS	-
dc.citation.volume	53	-
dc.citation.number	75	-
dc.citation.startPage	10394	-
dc.citation.endPage	10397	-
dc.date.scptcdate	2018-10-01	-
dc.description.wostc	3	-
dc.description.scptc	3	-
dc.description.journalClass	1	-
dc.description.journalRegisteredClass	scie	-
dc.description.journalRegisteredClass	scopus	-
dc.subject.keywordPlus	ORGANIC-SYNTHESIS	-
dc.subject.keywordPlus	PALLADIUM	-
dc.subject.keywordPlus	ACTIVATION	-
dc.subject.keywordPlus	QUINAZOLINONES	-
dc.subject.keywordPlus	COPPER	-
dc.subject.keywordPlus	FUNCTIONALIZATION	-
dc.subject.keywordPlus	FLUORINATION	-
dc.subject.keywordPlus	AMINATION	-
dc.subject.keywordPlus	CATALYSIS	-
dc.subject.keywordPlus	AMIDES	-