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Volumn 81, Issue 9, 2008, Pages 1158-1165

Catalytic nucleophilic addition reaction to (2-furyl)carbene intermediates generated from carbonyl-ene-ynes

Author keywords

[No Author keywords available]

Indexed keywords

CARBENE; CARBENOIDS; DIHYDROFURAN; ENE-YNE; H BONDS; IN-SITU; NUCLEOPHILIC ADDITIONS;

EID: 58149307489     PISSN: 00092673     EISSN: 13480634     Source Type: Journal    
DOI: 10.1246/bcsj.81.1158     Document Type: Article
Times cited : (16)

References (92)
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    • The reaction of le with 10 equivalents of cyclopentadiene at room temperature afforded mono-cyclopropanated product in 88% yield for 1.5 h.
    • The reaction of le with 10 equivalents of cyclopentadiene at room temperature afforded mono-cyclopropanated product in 88% yield for 1.5 h.
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    • The structure of 18d was determined by NOE experiments. See the Supporting Information. The reaction of 17d with 1.1 equivalents of NaH at 0 °C for 15 min gave the cyclized N-phenyl- morpholin-2-one 18d in 43% yield. This indicates the structure of 17d is an N-adduct.
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    • For selected nucleophilic additions of organometallic compounds to conjugated Fischer-type carbene complexes, see:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.