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Volumn 50, Issue 32, 2011, Pages 7337-7341

Palladium-catalyzed C-C bond formation to construct 1,4-diketones under mild conditions

Author keywords

1,4 diketones; enolate coupling; Paal Knorr reaction; palladium; chloroketones

Indexed keywords

CATALYSIS; KETONES; OLEFINS; SUBSTITUTION REACTIONS;

EID: 79960903755     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201101638     Document Type: Article
Times cited : (65)

References (56)
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    • 4-Methoxyphenylacetone (1 a) and desyl chloride (2 a) were applied in this nucleophilic substitution reaction in the presence of NaHMDS, but no desired coupling product was observed. Even though the direct deprotonation of the α-CH proton of desyl chloride by the sodium 4-methoxyphenylacetone enolate did occur.
    • 4-Methoxyphenylacetone (1 a) and desyl chloride (2 a) were applied in this nucleophilic substitution reaction in the presence of NaHMDS, but no desired coupling product was observed. Even though the direct deprotonation of the α-CH proton of desyl chloride by the sodium 4-methoxyphenylacetone enolate did occur.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.