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ChemInform Abstract: Enantioselective Total Synthesis of (+)-Taxusin

✍ Scribed by Ryoma Hara; Takashi Furukawa; Hajime Kashima; Hiroyuki Kusama; Yoshiaki Horiguchi; Isao Kuwajima


Publisher
John Wiley and Sons
Year
2010
Weight
24 KB
Volume
30
Category
Article
ISSN
0931-7597

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ChemInform Abstract: Enantioselective To
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Total Synthesis of (Β±)-Taxusin. -The synthesis of the title compound (VI) starting from (I) is highlighted by 1.) remarkably effective eight-membered B ring cyclization leading to the C ring allyl ester-type tricyclic taxane skeleton(III) with the desired B ring conformation and C-9/C-10 stereochem

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Enantioselective Total Synthesis of (+)-Isoboonein. -Starting from the known optically active diol (I), derived via an asymmetric Diels-Alder reaction of dimethyl fumarate with cyclopentadiene, the key intermediate (II) is synthesized via a known approach applied to the racemic series. Further sele

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