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Cacchi, S., Palmieri, G. (1985) The palladium-catalyzed conjugate addition type reaction of 2-bromo-arylmercury compounds and 2-bromo-aryl iodides with α,β-enones: A new entry to 1-indanols. Journal of Organometallic Chemistry, 282 (1) doi:10.1016/0022-328x(85)87153-9

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Reference TypeJournal (article/letter/editorial)
TitleThe palladium-catalyzed conjugate addition type reaction of 2-bromo-arylmercury compounds and 2-bromo-aryl iodides with α,β-enones: A new entry to 1-indanols
JournalJournal of Organometallic Chemistry
AuthorsCacchi, S.Author
Palmieri, G.Author
Year1985 (February)Volume282
Issue1
PublisherElsevier BV
DOIdoi:10.1016/0022-328x(85)87153-9Search in ResearchGate
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Mindat Ref. ID14464025Long-form Identifiermindat:1:5:14464025:8
GUID0
Full ReferenceCacchi, S., Palmieri, G. (1985) The palladium-catalyzed conjugate addition type reaction of 2-bromo-arylmercury compounds and 2-bromo-aryl iodides with α,β-enones: A new entry to 1-indanols. Journal of Organometallic Chemistry, 282 (1) doi:10.1016/0022-328x(85)87153-9
Plain TextCacchi, S., Palmieri, G. (1985) The palladium-catalyzed conjugate addition type reaction of 2-bromo-arylmercury compounds and 2-bromo-aryl iodides with α,β-enones: A new entry to 1-indanols. Journal of Organometallic Chemistry, 282 (1) doi:10.1016/0022-328x(85)87153-9
In(1985, February) Journal of Organometallic Chemistry Vol. 282 (1) Elsevier BV

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Cacchi, S., La Torre, F., Palmieri, G. (1984) The palladium-catalyzed conjugate addition type reaction of aryl iodides with α,β-unsaturated aldehydes. Journal of Organometallic Chemistry, 268 (2) doi:10.1016/0022-328x(84)80252-1
CACCHI, S., PALMIERI, G. (1984) ChemInform Abstract: THE PALLADIUM-CATALYZED CONJUGATE ADDITION TYPE REACTION OF 2-(N-ACYLAMINO)ARYLMERCURY COMPOUNDS WITH α,β-ENONES: A NEW ENTRY TO THE QUINOLINE SKELETON. Chemischer Informationsdienst, 15 (5) doi:10.1002/chin.198405204
CACCHI, S., LA TORRE, F., PALMIERI, G. (1984) ChemInform Abstract: THE PALLADIUM-CATALYZED CONJUGATE ADDITION TYPE REACTION OF ARYL IODIDES WITH α,β-UNSATURATED ALDEHYDES. Chemischer Informationsdienst, 15 (46) doi:10.1002/chin.198446112
CACCHI, S., MISITI, D., PALMIERI, G. (1981) ChemInform Abstract: THE PALLADIUM-CATALYZED CONJUGATE ADDITION TYPE REACTION OF ARYLMERCURY COMPOUNDS WITH α,β-UNSATURATED KETONES IN A TWO-PHASE SYSTEM. Chemischer Informationsdienst, 12 (47) doi:10.1002/chin.198147128
CACCHI, S., ARCADI, A. (1984) ChemInform Abstract: PALLADIUM-CATALYZED CONJUGATE ADDITION REACTION OF ARYL IODIDES WITH α,β-UNSATURATED KETONES. Chemischer Informationsdienst, 15 (18) doi:10.1002/chin.198418088
CACCHI, S., MISITI, D., PALMIERI, G. (1982) ChemInform Abstract: PALLADIUM-CATALYZED CONJUGATE ADDITION TYPE REACTION OF (2-HYDROXYARYL)MERCURY CHLORIDES WITH α,β-UNSATURATED KETONES IN A TWO-PHASE SYSTEM. A NEW SYNTHESIS OF 2-CHROMANOLS AND 2-CHROMENES. Chemischer Informationsdienst, 13 (52) doi:10.1002/chin.198252231
CACCHI, S., PALMIERI, G. (1984) ChemInform Abstract: A ONE-POT PALLADIUM-CATALYZED SYNTHESIS OF β,β-DIARYL KETONES AND ALDEHYDES FROM ARYL IODIDES AND α,β-UNSATURATED CARBONYL COMPOUNDS. Chemischer Informationsdienst, 15 (49) doi:10.1002/chin.198449143
Arcadi, A., Marinelli, F., Cacchi, S. (1986) The reaction of aryl iodides with hindered α,β,γ,δ-dienones in the presence of the [Pd(OAc)2(PPh3)2]-trialkylammonium formate reagent. Journal of Organometallic Chemistry, 312 (2) doi:10.1016/0022-328x(86)80306-0
Imamoto, Tsuneo, Sugiura, Yasushi (1985) Selective 1,2-addition of organocerium(III) reagents to α,β-unsaturated carbonyl compounds. Journal of Organometallic Chemistry, 285 (1) doi:10.1016/0022-328x(85)87395-2
Wakita, Yoshiaki, Yasunaga, Tomoyuki, Kojima, Masaharu (1985) Carbonylative cross-coupling reaction of aryl iodides with alkylaluminums by palladium complex catalysis. Journal of Organometallic Chemistry, 288 (3) 261-268 doi:10.1016/0022-328x(85)80118-2
Lee, Hye Kyung, Cho, Chan Sik (2012) Palladium-catalyzed cyclization of β-bromo-α,β-unsaturated ketones with arylhydrazines leading to 3-substituted 1-aryl-1 H -pyrazoles. Applied Organometallic Chemistry, 26 (11). 570-575 doi:10.1002/aoc.2900
 
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