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Volumn , Issue 6, 1999, Pages 744-746

Alkene chemoselectivity in ring-closing metathesis: A formal synthesis of (-)-periplanone-B

Author keywords

Alkenyl iodide; Alkenyl stannane; Metathesis; Organochromium; Palladium catalysis

Indexed keywords

PERIPLANONE B; PHEROMONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0033056177     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-2723     Document Type: Article
Times cited : (22)

References (30)
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    • 2Ru=CHPh under preferred conditions for RCM (ref. 10) resulted only in dimerisation [44% (E : Z = 73 : 27), 61% based on recovered triene] arising from metathesis at the the terminal (monoalkylsubstituted) alkene. Very recently, Grubbs has reported an imidazolinylidine-Ru catalyst which may be more effective: Scholl, M.; Trnka, T. M.; Morgan, J. P.; Grubbs, R. H. Tetrahedron Lett. 1999, 40, 2247-2250.
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    • i) compared with alcohol 9 could arise during preparation and/or Cr(II)-coupling of the aldehyde 14.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.