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Volumn 43, Issue 43, 2004, Pages 5821-5823

Total synthesis of apicularen a through transannular pyran formation

Author keywords

Cross coupling; Enamides; Macrolactonization; Total synthesis; Transannulation

Indexed keywords

BIOCHEMISTRY; ESTERIFICATION; ETHERS; SYNTHESIS (CHEMICAL); VINYL RESINS;

EID: 8844235688     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200460760     Document Type: Article
Times cited : (59)

References (42)
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  • 28
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    • note
    • The corresponding vinyl boronic acid (bis(triethylsilyl ether) derivative) obtained in 57% yield did not give the coupling product upon treatment with the triflate 12.
  • 32
    • 8844236365 scopus 로고    scopus 로고
    • note
    • 2, 0°C, 20 min, then -78°C, add 16, 1 h (34%)) the cyclization was accompanied by side reactions, such as ether cleavage.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.