Highly efficient syntheses of the anti‐cancer agent trans‐β‐elemene have been achieved by using the readily available (±)‐limonene as starting material. The syntheses were achieved in only nine to eleven steps with good overall yields. The k...
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https://www.riss.kr/link?id=O119033636
2018년
-
1434-193X
1099-0690
SCI;SCIE;SCOPUS
학술저널
4926-4932 [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
Highly efficient syntheses of the anti‐cancer agent trans‐β‐elemene have been achieved by using the readily available (±)‐limonene as starting material. The syntheses were achieved in only nine to eleven steps with good overall yields. The k...
Highly efficient syntheses of the anti‐cancer agent trans‐β‐elemene have been achieved by using the readily available (±)‐limonene as starting material. The syntheses were achieved in only nine to eleven steps with good overall yields. The key step in these reaction sequences is a stereoselective radical cyclization, induced by titanocene chloride.
Highly efficient syntheses of the anti‐cancer agent trans‐β‐elemene have been achieved by using the readily available (±)‐limonene as starting material. The syntheses were achieved in only nine to eleven steps with good overall yields. The key step in these reaction sequences is a stereoselective radical cyclization, induced by titanocene chloride.
Cobalt(II)‐Catalyzed N‐Acylation of Amines through a Transamidation Reaction
Discrimination of the Chirality of α‐Amino Acids in ZnII Complexes of DPA‐Appended Binaphthyl Imine