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

^*Corresponding author for this work

Department of Applied Chemistry

Research output: Contribution to journal › Article › peer-review

19 Scopus citations

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.

Original language	English
Pages (from-to)	3895-3896
Number of pages	2
Journal	Tetrahedron Letters
Volume	25
Issue number	35
DOIs	https://doi.org/10.1016/S0040-4039(01)91197-9
State	Published - 1 Jan 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",

month = jan,

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

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A new strategy for construction of angularly fused tricyclic ring systems. Transannular bond formation of bicyclic enones via photochemical intramolecular hydrogen abstraction. / Tobe, Yoshito; Iseki, Takayuki; Kakiuchi, Kiyomi et al.

In: Tetrahedron Letters, Vol. 25, No. 35, 01.01.1984, p. 3895-3896.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - A new strategy for construction of angularly fused tricyclic ring systems. Transannular bond formation of bicyclic enones via photochemical intramolecular hydrogen abstraction

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

SN - 0040-4039

VL - 25

SP - 3895

EP - 3896

JO - Tetrahedron Letters

JF - Tetrahedron Letters

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

Abstract

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