2007
DOI: 10.1002/anie.200703034
|View full text |Cite
|
Sign up to set email alerts
|

Creating a Reactive Enediyne by Using Visible Light: Photocontrol of the Bergman Cyclization

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
39
0
1

Year Published

2011
2011
2022
2022

Publication Types

Select...
5
5

Relationship

0
10

Authors

Journals

citations
Cited by 79 publications
(40 citation statements)
references
References 38 publications
0
39
0
1
Order By: Relevance
“…568 reaction with a dienophile to generate diarylethene derivatives 314a and 315a, which cyclize upon irradiation with UV light. The photogenerated 314b and 315b can be stably isolated and become inactive to the retro-Diels−Alder reaction.…”
Section: Chemical Reactivity and Bioactivitymentioning
confidence: 99%
“…568 reaction with a dienophile to generate diarylethene derivatives 314a and 315a, which cyclize upon irradiation with UV light. The photogenerated 314b and 315b can be stably isolated and become inactive to the retro-Diels−Alder reaction.…”
Section: Chemical Reactivity and Bioactivitymentioning
confidence: 99%
“…In the last few years, the Branda's group has pioneered the use of UCNPs to remotely control the photochemical response of dithienylethenes (DTEs), a class of photoswitchable molecules, which can reversibly interchange between two structural and electronic isomers upon UV and visible light (see Figure ). Furthermore, the high stability of DTEs and the durability of their photochemical behavior assure their usage for several cycles—an ideal feature for application in optical data storage, photorelease, and PDT …”
Section: Harvesting and Emitting Light With Inorganic Nanoparticlesmentioning
confidence: 99%
“…By taking advantage of visible-light molecular photoswitch, Sud et al [73] synthesized some thiophene-containing enediynes (at ene position) for BC. Lowmolecular-weight organic gelator-based, and amide-functionalized (phenylethynyl)thiophenes [74] were synthesized which were capable of immobilizing a variety of organic solvents to form stable organogels.…”
Section: 2mentioning
confidence: 99%