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Enantioselective formal synthesis of antitumor agent (+)-ottelione A

✍ Scribed by Mi Young Lee; Kyung Hwa Kim; Shuai Jiang; Yoo Hyun Jung; Jae Yi Sim; Geum-Sook Hwang; Do Hyun Ryu

Publisher
Elsevier Science
Year
2008
Tongue
French
Weight
111 KB
Volume
49
Category
Article
ISSN
0040-4039

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✦ Synopsis

The enantioselective formal synthesis of a natural antitumor product, (+)-ottelione A, was achieved through a catalytic enantioselective Diels-Alder strategy. These endeavors have led to the synthesis of a variety of synthetic analogues of this biologically potent natural product.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Enantioselective To
ChemInform Abstract: Enantioselective Total Synthesis of (+)-Ottelione A (I), (-)-Ottelione B (II), (+)-3-epi-Ottelione A (III) and Preliminary Evaluation of Their Antitumor Activity.
✍ Hiroshi Araki; Munenori Inoue; Takeyuki Suzuki; Takao Yamori; Michiaki Kohno; Ka πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons βš– 21 KB πŸ‘ 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a β€œFull Text” option. The original article is trackable v