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Volumn 130, Issue 15, 2008, Pages 5368-5377

Total synthesis of the Strychnos alkaloid (+)-minfiensine: Tandem enantioselective intramolecular Heck-iminium ion cyclization

Author keywords

[No Author keywords available]

Indexed keywords

INTRAMOLECULAR CHEMISTRY; STRYCHNOS ALKALOID MINFIENSINE; TOTAL SYNTHESIS; VINCORINE;

EID: 42149168996     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja800163v     Document Type: Article
Times cited : (180)

References (74)
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    • 2Me react to some extent under these conditions.
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    • This compound was not isolated in isomerically pure form, as it contained traces of other diene isomers
    • This compound was not isolated in isomerically pure form, as it contained traces of other diene isomers.
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    • Enantiomer ratios were determined by enantioselective HPLC analysis of tetracyclic product 27.
    • Enantiomer ratios were determined by enantioselective HPLC analysis of tetracyclic product 27.
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    • 3, this product reverted back to dienone 54.
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    • Some starting material remained in this reaction
    • Some starting material remained in this reaction.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.