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Volumn , Issue 10, 2001, Pages 1883-1886

Anionically induced domino reactions - Synthesis of a norpatchoulenol-type terpene

Author keywords

Alkenes; Domino reactions; Metathesis; Natural products; Oxidations

Indexed keywords

ALKENE; ANION; BICYCLO[2.2.2]OCTANE DERIVATIVE; NORPATCHOULENOL; TERPENE; TRICYCLO[5.3.1.0 3,8]UNDECANOLE; TRICYCLO[5.3.1.0 8,3]UNDECANONE; UNCLASSIFIED DRUG;

EID: 0035025890     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200105)2001:10<1883::AID-EJOC1883>3.0.CO;2-M     Document Type: Article
Times cited : (9)

References (22)
  • 7
    • 0342761156 scopus 로고
    • Studies in Natural Products Chemistry, (Ed.: Atta-ur-Rahman), Elsevier Amsterdam, Oxford, New York, Tokyo
    • D. Spitzner, in: Studies in Natural Products Chemistry, vol 8, Stereoselective Synthesis (Part E) (Ed.: Atta-ur-Rahman), Elsevier Amsterdam, Oxford, New York, Tokyo, 1991, p. 409-431.
    • (1991) Stereoselective Synthesis (Part E) , vol.8 , pp. 409-431
    • Spitzner, D.1
  • 21
    • 20644446370 scopus 로고    scopus 로고
    • This catalyst was a gift from BASF AG, Ludwigshafen (Rhein), Germany
    • This catalyst was a gift from BASF AG, Ludwigshafen (Rhein), Germany.
  • 22
    • 20644438980 scopus 로고    scopus 로고
    • note
    • The GC-MS shows several mono deoxygenated open chain products. We have no explanation for this unwanted reaction. The bulky TMS group, however, may have a beneficial conformational effect in the metathesis reaction (pre-organization of the substrate). We thank one of the referees for drawing our attention to this possibility.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.