A new strategy for construction of angularly fused tricyclic ring systems. Transannular bond formation of bicyclic enones via photochemical intramolecular hydrogen abstraction

Yoshito Tobe; Takayuki Iseki; Kiyomi Kakiuchi; Yoshinobu Odaira

doi:10.1016/S0040-4039(01)91197-9

A new strategy for construction of angularly fused tricyclic ring systems. Transannular bond formation of bicyclic enones via photochemical intramolecular hydrogen abstraction

Yoshito Tobe^*, Takayuki Iseki, Kiyomi Kakiuchi, Yoshinobu Odaira

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應用化學系

研究成果: Article › 同行評審

19 引文斯高帕斯（Scopus）

摘要

Tricyclic ketones 3a, b and 7a-c having angularly fused 5-6-5 or 5-7-5 ring system have been efficiently prepared by irradiation of bicyclic enones 1 and 2.

原文	English
頁（從 - 到）	3895-3896
頁數	2
期刊	Tetrahedron Letters
卷	25
發行號	35
DOIs	https://doi.org/10.1016/S0040-4039(01)91197-9
出版狀態	Published - 1 1月 1984

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10.1016/S0040-4039(01)91197-9

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title = "A new strategy for construction of angularly fused tricyclic ring systems. Transannular bond formation of bicyclic enones via photochemical intramolecular hydrogen abstraction",

abstract = "Tricyclic ketones 3a, b and 7a-c having angularly fused 5-6-5 or 5-7-5 ring system have been efficiently prepared by irradiation of bicyclic enones 1 and 2.",

author = "Yoshito Tobe and Takayuki Iseki and Kiyomi Kakiuchi and Yoshinobu Odaira",

year = "1984",

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doi = "10.1016/S0040-4039(01)91197-9",

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AU - Tobe, Yoshito

AU - Iseki, Takayuki

AU - Kakiuchi, Kiyomi

AU - Odaira, Yoshinobu

PY - 1984/1/1

Y1 - 1984/1/1

N2 - Tricyclic ketones 3a, b and 7a-c having angularly fused 5-6-5 or 5-7-5 ring system have been efficiently prepared by irradiation of bicyclic enones 1 and 2.

AB - Tricyclic ketones 3a, b and 7a-c having angularly fused 5-6-5 or 5-7-5 ring system have been efficiently prepared by irradiation of bicyclic enones 1 and 2.

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U2 - 10.1016/S0040-4039(01)91197-9

DO - 10.1016/S0040-4039(01)91197-9

M3 - Article

AN - SCOPUS:48749139913

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EP - 3896

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 35

ER -

A new strategy for construction of angularly fused tricyclic ring systems. Transannular bond formation of bicyclic enones via photochemical intramolecular hydrogen abstraction

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