1974
DOI: 10.1021/jo00931a034
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Reactions of cyclohexadienones. XXXII. Hydrogenolysis of carbon-carbon bonds in cyclohexadienones

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Cited by 15 publications
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“…alkylidenecyclopropanaones 34 and cyclohexadienones. 35,36 However, the activation of C sp 3 − C sp 3 σ bonds through a facile approach is rare. Recently, the metal-catalyzed C−C bond activation processes have earned increasing interest because of their high atom and step economy.…”
Section: ■ Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…alkylidenecyclopropanaones 34 and cyclohexadienones. 35,36 However, the activation of C sp 3 − C sp 3 σ bonds through a facile approach is rare. Recently, the metal-catalyzed C−C bond activation processes have earned increasing interest because of their high atom and step economy.…”
Section: ■ Introductionmentioning
confidence: 99%
“…The activation of C–X bonds (X = H, N, O, S, P, halogen) demands different synthetic strategies including variable temperature and/or tuned pressure, anaerobic atmosphere, , metal catalyst, strained ring system, , viz. alkylidenecyclopropanaones and cyclohexadienones. , However, the activation of C sp 3 –C sp 3 σ bonds through a facile approach is rare. Recently, the metal-catalyzed C–C bond activation processes have earned increasing interest because of their high atom and step economy .…”
Section: Introductionmentioning
confidence: 99%
“…Similar strategies have also been employed to achieve catalytic CCA of strained carbonyls or simple carbonyls assisted by chelation . Hydrogenolysis of C–C bonds catalyzed by transition metals has also been reported . However, these examples are limited to functionalized substrates.…”
mentioning
confidence: 99%