Cleavage of exo-7-substituted-6,8-dioxabicyclo[3.2.1]octanes with acetyl iodide in the predominance of the trans alkene product. This bicyclic ketal fragmentation methodology is utilized to a formal synthesis of sirenin.
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https://www.riss.kr/link?id=A101037097
1988
English
SCOPUS,KCI등재,SCIE
학술저널
135-136(2쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
Cleavage of exo-7-substituted-6,8-dioxabicyclo[3.2.1]octanes with acetyl iodide in the predominance of the trans alkene product. This bicyclic ketal fragmentation methodology is utilized to a formal synthesis of sirenin.
Cleavage of exo-7-substituted-6,8-dioxabicyclo[3.2.1]octanes with acetyl iodide in the predominance of the trans alkene product. This bicyclic ketal fragmentation methodology is utilized to a formal synthesis of sirenin.
Effect of Potassium Promoter on the Adsorption of Carbon Monoxide on Silica Supported Ruthenium
Reactions of Thianthrene Cation radical Perchlorate with 1-Alkyl-4-Arenesulfonylaminobenzenes