Photo-regulated cyclization reactions of tetraazamacrocycles with azobenzene derivatives

Wen Hao Wei; Takenori Tomohiro; Masato Kodaka; Hiroaki Okuno

doi:10.1039/a907030c

Photo-regulated cyclization reactions of tetraazamacrocycles with azobenzene derivatives

Wen Hao Wei, Takenori Tomohiro^*, Masato Kodaka, Hiroaki Okuno

^*Corresponding author for this work

Biorecognition Chemistry

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

3 Scopus citations

Abstract

The cyclization reaction between 1 and 2 was carried out in high dilution and was photochemically regulated to give 1:1 (29-33 membered rings, 52-55%) and 2:2 (58-66 membered rings, 20-49%) adducts as photo-controllable compounds.

Original language	English
Pages (from-to)	3397-3398
Number of pages	2
Journal	Journal of the Chemical Society - Perkin Transactions 1
Issue number	23
DOIs	https://doi.org/10.1039/a907030c
State	Published - 1999/12/07

ASJC Scopus subject areas

General Chemistry

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@article{b830b7af89294999a399886edf8663db,

title = "Photo-regulated cyclization reactions of tetraazamacrocycles with azobenzene derivatives",

abstract = "The cyclization reaction between 1 and 2 was carried out in high dilution and was photochemically regulated to give 1:1 (29-33 membered rings, 52-55%) and 2:2 (58-66 membered rings, 20-49%) adducts as photo-controllable compounds.",

author = "Wei, {Wen Hao} and Takenori Tomohiro and Masato Kodaka and Hiroaki Okuno",

year = "1999",

month = dec,

day = "7",

doi = "10.1039/a907030c",

language = "英語",

pages = "3397--3398",

journal = "Journal of the Chemical Society - Perkin Transactions 1",

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publisher = "ROYAL SOC CHEMISTRY",

number = "23",

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T1 - Photo-regulated cyclization reactions of tetraazamacrocycles with azobenzene derivatives

AU - Wei, Wen Hao

AU - Tomohiro, Takenori

AU - Kodaka, Masato

AU - Okuno, Hiroaki

PY - 1999/12/7

Y1 - 1999/12/7

N2 - The cyclization reaction between 1 and 2 was carried out in high dilution and was photochemically regulated to give 1:1 (29-33 membered rings, 52-55%) and 2:2 (58-66 membered rings, 20-49%) adducts as photo-controllable compounds.

AB - The cyclization reaction between 1 and 2 was carried out in high dilution and was photochemically regulated to give 1:1 (29-33 membered rings, 52-55%) and 2:2 (58-66 membered rings, 20-49%) adducts as photo-controllable compounds.

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U2 - 10.1039/a907030c

DO - 10.1039/a907030c

M3 - 学術論文

AN - SCOPUS:0003121361

SN - 0300-922X

SP - 3397

EP - 3398

JO - Journal of the Chemical Society - Perkin Transactions 1

JF - Journal of the Chemical Society - Perkin Transactions 1

IS - 23

ER -

Photo-regulated cyclization reactions of tetraazamacrocycles with azobenzene derivatives

Abstract

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