Synthesis of bicyclic dioxetanes tethering a fluororescer through an ω-carbamoyl-substituted linker and their high-performance chemiluminescence in an aqueous system-Reference-Cited by-同舟云学术

Synthesis of bicyclic dioxetanes tethering a fluororescer through an ω-carbamoyl-substituted linker and their high-performance chemiluminescence in an aqueous system

Published:2012-07 Issue:30 Volume:68 Page:6079-6087
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Watanabe Nobuko,Kino Hidetoshi,Watanabe Shinichiro,Ijuin Hisako K.,Yamada Masashi,Matsumoto Masakatsu

Funder

Ministry of Education, Culture, Sports, Science and Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference28 articles.

1. Chemiluminescence from a phenoxide-substituted 1,2-dioxetane: a model for firefly bioluminescence

2. Chemical and enzymatic triggering of 1,2-dioxetanes. 1: Aryl esterase-catalyzed chemiluminescence from a naphthyl acetate-substituted dioxetane

3. Chemical and enzymatic triggering of 1,2-dioxetanes. 2: fluoride-induced chemiluminescence from tert-butyldimethylsilyloxy-substituted dioxetanes

4. Reviews of dioxetane-based chemiluminescence, see:

5. Applications of dioxetane chemiluminescent probes to molecular biology

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