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Volumn 41, Issue 24, 2002, Pages 4732-4734

Selective isomerization of a terminal olefin catalyzed by a ruthenium complex: The synthesis of indoles through ring-closing metathesis

Author keywords

Heterocycles; Isomerization; Metathesis; Ring closure; Vinyls

Indexed keywords

CATALYSIS; ISOMERIZATION; RUTHENIUM; SYNTHESIS (CHEMICAL);

EID: 0037122126     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200290031     Document Type: Article
Times cited : (190)

References (39)
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    • Grubbs and co-workers found that vinylic ethers were not reactive in cross-metathesis. He also reported the formation of a new Fischer carbene species prepared by the reaction of a ruthenium-alkylidene complex with ethyl vinyl ether. (a) A. K. Chatterjee, J. P. Morgan, M. Scholl, R. H. Grubbs, J. Am. Chem. Soc. 2000, 122, 3783-3784; b) J. Louie, R. H. Grubbs, Organometallics 2002, 21, 2153-2164).
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    • Grubbs and co-workers found that vinylic ethers were not reactive in cross-metathesis. He also reported the formation of a new Fischer carbene species prepared by the reaction of a ruthenium-alkylidene complex with ethyl vinyl ether. (a) A. K. Chatterjee, J. P. Morgan, M. Scholl, R. H. Grubbs, J. Am. Chem. Soc. 2000, 122, 3783-3784; b) J. Louie, R. H. Grubbs, Organometallics 2002, 21, 2153-2164).
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    • Louie, J.1    Grubbs, R.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.