Organolithium and organomagnesium compounds of the naphthalene series in organic synthesis
Identifieur interne : 001278 ( Main/Exploration ); précédent : 001277; suivant : 001279Organolithium and organomagnesium compounds of the naphthalene series in organic synthesis
Auteurs :Source :
- Russian Chemical Reviews [ 0036-021X ] ; 2006-08-31.
Descripteurs français
English descriptors
- KwdEn :
- Alkyl, Analogue, Angew, Binaphthyl, Binaphthyls, Bromide, Bunli, Busli, Butli, Butyllithium, Carboxamide group, Chem, Clayden, Co2h, Compound, Derivative, Diethyl, Diethyl ether, Electrophile, Electrophiles, Engl, Equiv, Et2o, Gabba, Good results, Good yields, Grignard, Halide, Halogen, High temperature, Isomer, Ketone, Khim, Latter compound, Lett, Lithiation, Lithium, Lithium alkyls, Lithium atom, Lithium derivatives, Magnesium, Magnesium naphthalenes, Me2n, Me3si, Me3sicl, Metal halogen exchange, Metal naphthalenes, Metallated, Metallating, Metallating agent, Metallating agents, Metallation, Methoxy group, Meyers, Mgbr, Moiety, Naphthalene, Naphthalene derivatives, Naphthalene moiety, Naphthalene ring, Naphthalene series, Naphthol, Naphthyl, Naphthylmetals, Net2, Nme2, Npri2, Organic synthesis, Organolithium, Organomagnesium, Organomagnesium compounds, Organomet, Organometallic, Organometallic compounds, Organometallic derivatives, Organometallic reagents, Ortho, Ortho position, Peri, Peri position, Perkin trans, Pozharskii, Pph2, Pri2, Reaction conditions, Reaction mixture, Reagent, Room temperature, Ryabtsova, Schleyer, Sime3, Snieckus, Snieckus tetrahedron lett, Substituent, Substituents, Tetrahedron, Tmeda, Transition state, Various electrophiles.
- Teeft :
- Alkyl, Analogue, Angew, Binaphthyl, Binaphthyls, Bromide, Bunli, Busli, Butli, Butyllithium, Carboxamide group, Chem, Clayden, Co2h, Compound, Derivative, Diethyl, Diethyl ether, Electrophile, Electrophiles, Engl, Equiv, Et2o, Gabba, Good results, Good yields, Grignard, Halide, Halogen, High temperature, Isomer, Ketone, Khim, Latter compound, Lett, Lithiation, Lithium, Lithium alkyls, Lithium atom, Lithium derivatives, Magnesium, Magnesium naphthalenes, Me2n, Me3si, Me3sicl, Metal halogen exchange, Metal naphthalenes, Metallated, Metallating, Metallating agent, Metallating agents, Metallation, Methoxy group, Meyers, Mgbr, Moiety, Naphthalene, Naphthalene derivatives, Naphthalene moiety, Naphthalene ring, Naphthalene series, Naphthol, Naphthyl, Naphthylmetals, Net2, Nme2, Npri2, Organic synthesis, Organolithium, Organomagnesium, Organomagnesium compounds, Organomet, Organometallic, Organometallic compounds, Organometallic derivatives, Organometallic reagents, Ortho, Ortho position, Peri, Peri position, Perkin trans, Pozharskii, Pph2, Pri2, Reaction conditions, Reaction mixture, Reagent, Room temperature, Ryabtsova, Schleyer, Sime3, Snieckus, Snieckus tetrahedron lett, Substituent, Substituents, Tetrahedron, Tmeda, Transition state, Various electrophiles.
Url:
DOI: 10.1070/RC2006v075n08ABEH003611
Affiliations:
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Le document en format XML
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Alkyl</term>
<term>Analogue</term>
<term>Angew</term>
<term>Binaphthyl</term>
<term>Binaphthyls</term>
<term>Bromide</term>
<term>Bunli</term>
<term>Busli</term>
<term>Butli</term>
<term>Butyllithium</term>
<term>Carboxamide group</term>
<term>Chem</term>
<term>Clayden</term>
<term>Co2h</term>
<term>Compound</term>
<term>Derivative</term>
<term>Diethyl</term>
<term>Diethyl ether</term>
<term>Electrophile</term>
<term>Electrophiles</term>
<term>Engl</term>
<term>Equiv</term>
<term>Et2o</term>
<term>Gabba</term>
<term>Good results</term>
<term>Good yields</term>
<term>Grignard</term>
<term>Halide</term>
<term>Halogen</term>
<term>High temperature</term>
<term>Isomer</term>
<term>Ketone</term>
<term>Khim</term>
<term>Latter compound</term>
<term>Lett</term>
<term>Lithiation</term>
<term>Lithium</term>
<term>Lithium alkyls</term>
<term>Lithium atom</term>
<term>Lithium derivatives</term>
<term>Magnesium</term>
<term>Magnesium naphthalenes</term>
<term>Me2n</term>
<term>Me3si</term>
<term>Me3sicl</term>
<term>Metal halogen exchange</term>
<term>Metal naphthalenes</term>
<term>Metallated</term>
<term>Metallating</term>
<term>Metallating agent</term>
<term>Metallating agents</term>
<term>Metallation</term>
<term>Methoxy group</term>
<term>Meyers</term>
<term>Mgbr</term>
<term>Moiety</term>
<term>Naphthalene</term>
<term>Naphthalene derivatives</term>
<term>Naphthalene moiety</term>
<term>Naphthalene ring</term>
<term>Naphthalene series</term>
<term>Naphthol</term>
<term>Naphthyl</term>
<term>Naphthylmetals</term>
<term>Net2</term>
<term>Nme2</term>
<term>Npri2</term>
<term>Organic synthesis</term>
<term>Organolithium</term>
<term>Organomagnesium</term>
<term>Organomagnesium compounds</term>
<term>Organomet</term>
<term>Organometallic</term>
<term>Organometallic compounds</term>
<term>Organometallic derivatives</term>
<term>Organometallic reagents</term>
<term>Ortho</term>
<term>Ortho position</term>
<term>Peri</term>
<term>Peri position</term>
<term>Perkin trans</term>
<term>Pozharskii</term>
<term>Pph2</term>
<term>Pri2</term>
<term>Reaction conditions</term>
<term>Reaction mixture</term>
<term>Reagent</term>
<term>Room temperature</term>
<term>Ryabtsova</term>
<term>Schleyer</term>
<term>Sime3</term>
<term>Snieckus</term>
<term>Snieckus tetrahedron lett</term>
<term>Substituent</term>
<term>Substituents</term>
<term>Tetrahedron</term>
<term>Tmeda</term>
<term>Transition state</term>
<term>Various electrophiles</term>
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<keywords scheme="Teeft" xml:lang="en"><term>Alkyl</term>
<term>Analogue</term>
<term>Angew</term>
<term>Binaphthyl</term>
<term>Binaphthyls</term>
<term>Bromide</term>
<term>Bunli</term>
<term>Busli</term>
<term>Butli</term>
<term>Butyllithium</term>
<term>Carboxamide group</term>
<term>Chem</term>
<term>Clayden</term>
<term>Co2h</term>
<term>Compound</term>
<term>Derivative</term>
<term>Diethyl</term>
<term>Diethyl ether</term>
<term>Electrophile</term>
<term>Electrophiles</term>
<term>Engl</term>
<term>Equiv</term>
<term>Et2o</term>
<term>Gabba</term>
<term>Good results</term>
<term>Good yields</term>
<term>Grignard</term>
<term>Halide</term>
<term>Halogen</term>
<term>High temperature</term>
<term>Isomer</term>
<term>Ketone</term>
<term>Khim</term>
<term>Latter compound</term>
<term>Lett</term>
<term>Lithiation</term>
<term>Lithium</term>
<term>Lithium alkyls</term>
<term>Lithium atom</term>
<term>Lithium derivatives</term>
<term>Magnesium</term>
<term>Magnesium naphthalenes</term>
<term>Me2n</term>
<term>Me3si</term>
<term>Me3sicl</term>
<term>Metal halogen exchange</term>
<term>Metal naphthalenes</term>
<term>Metallated</term>
<term>Metallating</term>
<term>Metallating agent</term>
<term>Metallating agents</term>
<term>Metallation</term>
<term>Methoxy group</term>
<term>Meyers</term>
<term>Mgbr</term>
<term>Moiety</term>
<term>Naphthalene</term>
<term>Naphthalene derivatives</term>
<term>Naphthalene moiety</term>
<term>Naphthalene ring</term>
<term>Naphthalene series</term>
<term>Naphthol</term>
<term>Naphthyl</term>
<term>Naphthylmetals</term>
<term>Net2</term>
<term>Nme2</term>
<term>Npri2</term>
<term>Organic synthesis</term>
<term>Organolithium</term>
<term>Organomagnesium</term>
<term>Organomagnesium compounds</term>
<term>Organomet</term>
<term>Organometallic</term>
<term>Organometallic compounds</term>
<term>Organometallic derivatives</term>
<term>Organometallic reagents</term>
<term>Ortho</term>
<term>Ortho position</term>
<term>Peri</term>
<term>Peri position</term>
<term>Perkin trans</term>
<term>Pozharskii</term>
<term>Pph2</term>
<term>Pri2</term>
<term>Reaction conditions</term>
<term>Reaction mixture</term>
<term>Reagent</term>
<term>Room temperature</term>
<term>Ryabtsova</term>
<term>Schleyer</term>
<term>Sime3</term>
<term>Snieckus</term>
<term>Snieckus tetrahedron lett</term>
<term>Substituent</term>
<term>Substituents</term>
<term>Tetrahedron</term>
<term>Tmeda</term>
<term>Transition state</term>
<term>Various electrophiles</term>
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<term>Magnésium</term>
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