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Volumn 47, Issue 13, 2006, Pages 2103-2106

Construction of spiro[5.5]undecanes containing a quaternary carbon atom adjacent to a spirocentre via an Ireland ester Claisen rearrangement and RCM reaction sequence. Total syntheses of (±)-α-chamigrene, (±)-β-chamigrene and (±)-laurencenone C

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA CHAMIGRENE; BETA CHAMIGRENE; LAURENCENONE; NATURAL PRODUCT; UNCLASSIFIED DRUG;

EID: 33344467238     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.01.131     Document Type: Article
Times cited : (23)

References (27)
  • 12
    • 0026085988 scopus 로고
    • 13C spectral data for synthetic (±)-α-chamigrene reported by these authors is quite different from those reported by others. See: J. Plamondon, and P. Canonne Tetrahedron Lett. 32 1991 589 592
    • (1991) Tetrahedron Lett. , vol.32 , pp. 589-592
    • Plamondon, J.1    Canonne, P.2
  • 24
    • 33344475843 scopus 로고    scopus 로고
    • note
    • It is worth noting that the Wittig reaction of norchamigrenone under standard conditions or with tert-amyl oxide in the absence of tert-amyl alcohol furnished a very poor yield of β-chamigrene.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.