1965
DOI: 10.1021/ja01079a030
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Geometric Isomers of Methylenes

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1968
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Cited by 54 publications
(46 citation statements)
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(1 reference statement)
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“…The very small D value reported for 9-anthrylcarbene (7a) 61 indicates great ability to delocalize unpaired electrons, thus supporting theoretical predictions. 5.2.3.1.…”
Section: Anthrylcarbenessupporting
confidence: 64%
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“…The very small D value reported for 9-anthrylcarbene (7a) 61 indicates great ability to delocalize unpaired electrons, thus supporting theoretical predictions. 5.2.3.1.…”
Section: Anthrylcarbenessupporting
confidence: 64%
“…61 The ESR spectra of the -isomer ( -62b) also consisted of two sets of triplet peaks of similar intensities, assignable to Z and E rotamers. However, only one set of triplet signals was observed in the ESR spectra of R-62b under the same conditions.…”
Section: Naphthylcarbenesmentioning
confidence: 97%
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“…Only one thioxocarbene and a few closely related iminocarbene triplets have been detected by ESR to date, The existence of geometric isomers in triplet carbenes, initially observed in naphthylmethylenes by Trozzolo et al [41], has been extensively studied and recently reviewed by Roth and coworkers [28]. Here we will only present the essential principles underlying the assignment of the two sets of signals to each individual isomer, on the basis of Roth's pioneering work.…”
Section: = Os Nrmentioning
confidence: 96%
“…[1] As a singlet carbene [2] and the most stable dihalocarbene, [1d] difluorocarbene shows moderate electrophilicity due to both strong inductive effect and electron-donating resonance effect induced by fluorine. The understanding of its reactivity has led to a variety of novel organic transformations, [1] including difluoromethylation, [3] trifluoromethylation, [4] and [2+1] cycloaddition [3a] .…”
mentioning
confidence: 99%