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Volumn 9, Issue 10, 2007, Pages 1951-1954

A new construction of 2-alkoxypyrans by an acylation-reductive cyclization sequence

Author keywords

[No Author keywords available]

Indexed keywords

ACUTIPHYCIN; BRYOSTATIN 1; HETEROCYCLIC COMPOUND; MACROLIDE; PYRAN DERIVATIVE; UNCLASSIFIED DRUG;

EID: 34249316162     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol070573h     Document Type: Article
Times cited : (23)

References (32)
  • 22
    • 0037670118 scopus 로고    scopus 로고
    • For an isolated example of a related cyclization using an unfunctionalized saturated alkyl iodide, see
    • For an isolated example of a related cyclization using an unfunctionalized saturated alkyl iodide, see: Kawamura, K.; Hinou, H.; Matsuo, G.; Nakata, T. Tetrahedron Lett. 2003, 44, 5259.
    • (2003) Tetrahedron Lett , vol.44 , pp. 5259
    • Kawamura, K.1    Hinou, H.2    Matsuo, G.3    Nakata, T.4
  • 23
    • 34249289441 scopus 로고    scopus 로고
    • Since the reaction could be driven by steady addition of portions of dibromoethane, we attribute the low yields to a combination of a lack of adequate reactivity of the allyl chloride and surface activation of the magnesium; the reaction scale was 0.36 mmol of starting chloride
    • Since the reaction could be driven by steady addition of portions of dibromoethane, we attribute the low yields to a combination of a lack of adequate reactivity of the allyl chloride and surface activation of the magnesium; the reaction scale was 0.36 mmol of starting chloride.
  • 32
    • 34249285584 scopus 로고    scopus 로고
    • This macrolactonization procedure has been thoroughly optimized and care has also been taken to document the reproducibility of the yield for this reaction
    • This macrolactonization procedure has been thoroughly optimized and care has also been taken to document the reproducibility of the yield for this reaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.