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Volumn 43, Issue 41, 2002, Pages 7445-7448

A short and efficient synthetic approach to hydroxy (E)-stilbenoids via solid-phase cross metathesis

Author keywords

[No Author keywords available]

Indexed keywords

3,4 DIACETOXY 4' HYDROXYSTILBENE; 4 HYDROXYSTILBENE; ETHER DERIVATIVE; RESVERATROL; STILBENE DERIVATIVE; STYRENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037037836     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01528-9     Document Type: Article
Times cited : (50)

References (37)
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    • Higher yields were obtained in this reaction when the solid supported substrate was swelled at least 2 h before addition of the carbene catalyst.
    • Higher yields were obtained in this reaction when the solid supported substrate was swelled at least 2 h before addition of the carbene catalyst.
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    • It is assumed that rather long and flexible olefinic moieties on resin allow site-site interactions leading to the intramolecular metathesis as in Ref. 14. However, extents of those interactions may be much less in the bound styrenyl double bonds probably due to steric reasons.
    • It is assumed that rather long and flexible olefinic moieties on resin allow site-site interactions leading to the intramolecular metathesis as in Ref. 14 . However, extents of those interactions may be much less in the bound styrenyl double bonds probably due to steric reasons.
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    • Aliphatic olefins (e.g. 1-hexene) were also reacted with the resin bound styrenyl ether with similar efficiency under otherwise identical conditions.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.