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Volumn , Issue 20-21, 2011, Pages 3634-3647

Progress in metathesis through natural product synthesis

Author keywords

Alkenes; Alkynes; Medium ring compounds; Metathesis; Natural products; Synthesis design

Indexed keywords


EID: 79960297458     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201100442     Document Type: Review
Times cited : (105)

References (120)
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    • For another example of RCM of epimers leading to cyclooctenes that is only successful in the case of the configuration corresponding to the natural product, see:, R. Mizutani, K. Nakashima, Y. Saito, M. Sono, M. Tori, Tetrahedron Lett. 2009, 50, 2225.
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    • For the effect of titanium isopropoxide on the E/Z selectivity of a RCM leading to a cyclodecene, see M. Nevalainen, A. M. P. Koskinen, Angew. Chem. 2001, 113, 4184;
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    • For another example of the importance of the disconnection site, in the RCM leading to the cyclononene core of the cornexistins, see:, J. S. Clark, F. Martin, B. Nay, C. Wilson, Org. Lett. 2003, 5, 89.
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    • A. Vincent, J. Prunet, unpublished results. For another demanding CM leading to a trisubstituted double bond, see
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.