2009
DOI: 10.1039/b911228f
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Visible light driven room temperature Pauson–Khand reaction

Abstract: Visible light driven decarbonylation of [(mu(2)-alkyne)Co(2)(CO)(6)] complexes enables the formation of cyclopentenones in good yields at ambient temperatures.

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Cited by 14 publications
(9 citation statements)
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“…Pauson–Khand reactions are often applied to prepare cyclopentenone scaffolds by cocyclization of alkynes, alkenes and CO. The decarbonylation step from an alkyne-cobalt complex can be promoted thermally, but an improved functional group tolerance can be obtained with other activation methods such as microwave, ultrasound, and especially light irradiation . Asano and Yoshida reported a microflow protocol for the photoinitiated Pauson–Khand reaction .…”
Section: Continuous-flow Photochemistry In Organic Synthesismentioning
confidence: 99%
“…Pauson–Khand reactions are often applied to prepare cyclopentenone scaffolds by cocyclization of alkynes, alkenes and CO. The decarbonylation step from an alkyne-cobalt complex can be promoted thermally, but an improved functional group tolerance can be obtained with other activation methods such as microwave, ultrasound, and especially light irradiation . Asano and Yoshida reported a microflow protocol for the photoinitiated Pauson–Khand reaction .…”
Section: Continuous-flow Photochemistry In Organic Synthesismentioning
confidence: 99%
“…Reagents: All chemicals were purchased from commercial suppliers and were used as received. The synthesis of [Co 2 (CO) 6 (η 2 ‐Me 3 SiC≡CH)] was performed according to published procedures31–33 using some modifications to increase selectivity and yield.…”
Section: Methodsmentioning
confidence: 72%
“…Dicobaltatetrahedranes 3a-i have been synthesized according to published reaction procedures [35][36][37] which are modied to increase selectivity and yield. In this respect, dicobaltoctacarbonyl 1 was reacted with alkynes 2a-i in n-hexane at ambient temperature for 2 h (Scheme 1).…”
Section: Resultsmentioning
confidence: 99%
“…Compounds 3a-i were prepared in a modied reaction protocol according to published procedures. [35][36][37] All other chemicals were purchased from commercial suppliers and were used as received. Fig.…”
Section: Reagentsmentioning
confidence: 99%