1985
DOI: 10.1021/ja00290a053
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Two-alkyne annulations of transition-metal carbene complexes via in situ generated vinyl carbene complexes

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Cited by 76 publications
(22 citation statements)
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“…The reaction takes place with a high excess of a terminal alkyne 115 in THF providing only moderate yields of phenols 116 [50] (Scheme 21). This pattern of reactivity has also been encountered in the reaction of molybdenum carbene complex 1a (M = Mo, R 1 = Bu) with an 1,7-enyne (9% yield) [34].…”
Section: [2 + 2 + 1 + 1] Cyclization Involving Two Alkyne Units and Rmentioning
confidence: 99%
“…The reaction takes place with a high excess of a terminal alkyne 115 in THF providing only moderate yields of phenols 116 [50] (Scheme 21). This pattern of reactivity has also been encountered in the reaction of molybdenum carbene complex 1a (M = Mo, R 1 = Bu) with an 1,7-enyne (9% yield) [34].…”
Section: [2 + 2 + 1 + 1] Cyclization Involving Two Alkyne Units and Rmentioning
confidence: 99%
“…The synthetic potential of these multistep multicomponent cyclization reactions has not yet been fully explored, and there are examples of other potentially useful sequences such as the topologies [2+2+1+1], 914 giving bicyclo[3.1.0]lactams from chromium aminocarbene complexes and alkynes, or the inter- 850,868 or intramolecular 915 …”
Section: 859mentioning
confidence: 99%
“…The H NNR and IR spectra of the 3-methyl-5,6,7,8-tetrahydro-2-1 naphthol and 2,3-dihydro-6-methyl-IH-inden-5-ol are identical to those published. 5 The IH NMR spectra of the other products, all previously unknown, showed the resonances and intensitte. required.…”
Section: Chmentioning
confidence: 88%
“…(1-methoxyethylidene)tungsten, 5 or perhaps by losing a cis-ligand 7 and following a path via i or_. 2b,8…”
Section: It Is Not Clear What Accounts For the Reactivity Of The Metamentioning
confidence: 99%