2014
DOI: 10.1016/j.tetlet.2013.12.006
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Radical reaction of chlorophyll derivatives triggered by AIBN

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Cited by 7 publications
(4 citation statements)
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“…The Oba group performed the hydrothiolation of vinyl chlorin 21 by reacting with PhSH using AINB as a radical initiator (Scheme 14) 47. The reaction gave expected product 22a in 62% yield together with byproducts 22b-d.…”
mentioning
confidence: 99%
“…The Oba group performed the hydrothiolation of vinyl chlorin 21 by reacting with PhSH using AINB as a radical initiator (Scheme 14) 47. The reaction gave expected product 22a in 62% yield together with byproducts 22b-d.…”
mentioning
confidence: 99%
“…AIBN is widely known as a radical initiator. , However, recently, Han pioneered the application of AIBN as a “CN” source in the formation of C–CN bonds (Scheme , eq 1) . Subsequently, we described an S -cyanation reaction by AIBN (Scheme , eq 2) .…”
mentioning
confidence: 99%
“…On the other hand, FD increased sharply at times below 10 h, while the growth trend of FD gradually became inconspicuous as the time increased above 10 h, especially for the temperatures of 60, 70, and 80 °C. As we know, the half-life time of initiator AIBN was below 10 h at temperatures above 65 °C (e.g., t half‑life, AIBN ≈ 10 h at 65 °C, and ≈ 5 h at 70 °C); ,, thus, the relative lower concentration of AIBN led to a slower reaction rate.…”
Section: Resultsmentioning
confidence: 99%