H. Takeshita, 竹下 齊, I. Kouno, 河野 功, H. Iwabuchi, 岩渕 久克, M. Iino, 飯野 光明, D. Nomura, 野村 男次, ヒトシ タケシタ, イサオ コウノ, ヒサカツ イワブチ, ミツアキ イイノ, ダンジ ノムラ
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引用次数: 0
Abstract
An effective preparation of protoilludanes was developed by use of two-fold photocycloadditions and methylation. Stereochemistry of the photocycloaddition processes was clarified on the basis of chemical transformations as well as the NMR evidence. Taking an advantage of this facile formation of the natural protoilludane ring derivation, some of the biogenetically significant oxygenated derivatives have been totally synthesized.
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