2008
DOI: 10.1016/j.tet.2007.11.092
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Synthesis of six-membered oxygenated heterocycles through carbon–oxygen bond-forming reactions

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Cited by 243 publications
(76 citation statements)
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“…135 Generally, this reaction is promoted by electrophilic entities such as iodine, 136 phenylselenium chloride, 137 as well as mercuric 138 or palladium salts. 139 Nevertheless, a second step is needed in these processes to remove the electrophile.…”
Section: Intramolecular Hydroalkoxylation Of Olefinsmentioning
confidence: 99%
“…135 Generally, this reaction is promoted by electrophilic entities such as iodine, 136 phenylselenium chloride, 137 as well as mercuric 138 or palladium salts. 139 Nevertheless, a second step is needed in these processes to remove the electrophile.…”
Section: Intramolecular Hydroalkoxylation Of Olefinsmentioning
confidence: 99%
“…[1,2] (Figure 1). The piperidines resemble one of such important alkaloid cores mentioned for clinical and pre-clinical trials.…”
mentioning
confidence: 99%
“…The piperidines resemble one of such important alkaloid cores mentioned for clinical and pre-clinical trials. [1,2] (Figure 1). Thus,catalytic synthetic approaches towards synthesis of these nitrogen heterocycles are highly sought after.…”
mentioning
confidence: 99%
“…[1] Their partially hydrogenated derivatives, for example, 3,4-dihydropyrans, [2] are interesting precursors for tetrahydropyrans [3] and glycals, [4] which are useful building blocks, particularly in carbohydrate chemistry. [1] Their partially hydrogenated derivatives, for example, 3,4-dihydropyrans, [2] are interesting precursors for tetrahydropyrans [3] and glycals, [4] which are useful building blocks, particularly in carbohydrate chemistry.…”
mentioning
confidence: 99%