Sasaki et al., 1993 - Google Patents
Ni (0)-triphenylphosphine complex-catalyzed homo-coupling of 1-alkenyl halides with zinc powderSasaki et al., 1993
- Document ID
- 1309790360447812041
- Author
- Sasaki K
- Nakao K
- Kobayashi Y
- Sakai M
- Uchino N
- Sakakibara Y
- Takagi K
- Publication year
- Publication venue
- Bulletin of the Chemical Society of Japan
External Links
Snippet
The homo-coupling of 1-alkenyl halides was examined in the presence of NiBr2 (PPh3) 2, PPh3, and excess zinc. The reactions proceed under very mild conditions to give high yields of conjugated dienes. The addition of KI or thiourea was unnecessary for a successful …
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 C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 0 title abstract description 72
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- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
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- C07C1/321—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen the hetero-atom being a non-metal atom
- C07C1/323—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen the hetero-atom being a non-metal atom the hetero-atom being a nitrogen atom
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
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De La Rosa et al. | Cross-coupling reactions of monosubstituted acetylenes and aryl halides catalyzed by palladium on charcoal | |
Mckillop et al. | Organic synthesis using supported reagents-Part II | |
Bozell et al. | Bimetallic catalysis. A new method for the activation of chloroarenes toward palladium-catalyzed coupling with olefins | |
Fujisaki et al. | Halogenation Using N-Halogenocompounds. I. Effect of Amines on ortho-Bromination of Phenols with NBS. | |
Nozaki et al. | Acylcyanation of terminal acetylenes: palladium-catalyzed addition of aryloyl cyanides to arylacetylenes | |
Roberto et al. | Novel synthesis of pyrrolidinones by cobalt carbonyl catalyzed carbonylation of azetidines. A new ring-expansion-carbonylation reaction of 2-vinylazetidines to tetrahydroazepinones | |
Ciattini et al. | Palladium-catalyzed cross-coupling reactions of vinyl and aryl triflates with tetraarylborates | |
Catellani et al. | Selective aryl coupling via palladacycles: a new route to m-alkylbiphenyls or m-terphenyls | |
Birch et al. | Organometallic complexes in synthesis. Part IV. Abstraction of hydride from some tricarbonylcyclohexa-1, 3-dieneiron complexes and reactions of the complexed cations with some nucleophiles | |
Ashby et al. | Transition metal catalyzed reactions of lithium aluminum hydride with alkyl and aryl halides | |
Sasaki et al. | Ni (0)-triphenylphosphine complex-catalyzed homo-coupling of 1-alkenyl halides with zinc powder | |
TW369543B (en) | Process for the preparation of polyalkyl-1-oxa-diazaspirodecane compounds | |
Zhou et al. | Synthesis of pyrrolidines and pyrrolidinones by the rhodium complex catalyzed cyclization of unsaturated amines | |
Kikukawa et al. | Reaction of diazonium salts with transition metals. Part 13. Palladium-catalyzed carbonylative coupling of arenediazonium salts with organotin reagents to give aromatic ketones | |
Okano et al. | TRANSITION METAL PHOSPHINE COMPLEXES POSSESSING A PHASE TRANSFER FUNCTION. PREPARATION AND PROPERTIES OF POLYETHER-SUBSTITUTED PHOSPHINES AND THEIR PALLADIUM COMPLEXES | |
Witulski et al. | Chemo-and regioselective crossed alkyne cyclotrimerisation of 1, 6-diynes with terminal monoalkynes mediated by Grubbs’ catalyst or Wilkinson’s catalystElectronic supplementary information (ESI) available: experimental procedures and analytical data for 3, 4 and 5. See http://www. rsc. org/suppdata/cc/b0/b005636g | |
Gallina | Regio and stereospecific synthesis of cis and trans 3-methyl-6-methylethyl cyclohexenes and 3-methyl-4-methylethylcyclohexenes. Reactions of allylic acetates and carbamates with Li2Cu3Me5 and LiCuMe2 | |
Kleijn et al. | The palladium (0)‐catalysed formation of 3‐methoxy‐1, 3‐butadienes from methoxypropadiene derivatives and organozinc compounds | |
Williams et al. | Unexpected titanium shifts during cyclopropanation of N, N-dibenzylformamide with ligand-exchanged titanium-alkadiene complexes | |
Ando et al. | An N-heterocyclic carbene-based nickel catalyst for the Kumada–Tamao–Corriu coupling of aryl bromides and tertiary alkyl Grignard reagents | |
Fugami et al. | Novel palladium-catalyzed diarylation and dialkenylation reactions of norbornene derivatives | |
Makosza et al. | Reactions of organic anions. 120. Vicarious nucleophilic substitution of hydrogen in nitrophenols and polynitroarenes. Examples of nucleophilic addition to nitrocyclohexadienonenitronate anions | |
Alper et al. | Synthesis of fulvenes by reaction of thiobenzophenones with cyclopentadienylmetal carbonyl anions under anhydrous or phase transfer catalyzed conditions | |
Uemura et al. | Selenocyanatodethallation in organothallium (III) compounds | |
Quintana et al. | Decomposition of diazoketones in organic sulfides and sulfoxides: Cyclopropane formation from diazoketones via sulfonium ylides |