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Volumn 65, Issue 41, 2009, Pages 8542-8555

Regioselective access to substituted oxindoles via rhodium-catalyzed carbene C-H insertion

Author keywords

C H insertion; Carbene; Catalysis; Oxindole; Regioselective; Rhodium

Indexed keywords

2 SILYLOXYINDOLE 3 CARBOXYLATE DERIVATIVE; AROMATIC COMPOUND; AZO COMPOUND; CARBENE; DIETHYLAMINE; ESTER; OXINDOLE; RHODIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 69549108463     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.08.006     Document Type: Article
Times cited : (21)

References (113)
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    • Iodonium ylids can also react in the presence of rhodium or copper catalysts to afford metallacarbenes which can then insert into various C-H bonds with comparable selectivities
    • Iodonium ylids can also react in the presence of rhodium or copper catalysts to afford metallacarbenes which can then insert into various C-H bonds with comparable selectivities.
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    • It should be mentioned that acylation of the p-nitroaniline did not prove successful.
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    • Using the same strategy, we envisaged synthesizing the Weinreb amide analog of 14. Unfortunately, while the N,O-dimethyl diazoacetamide proved to be easily accessible, its reaction with triphosgene did not afford the expected acyl chloride.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.