Organolithium and organomagnesium compounds of the naphthalene series in organic synthesis

Identifieur interne : 001C19 ( Istex/Curation ); précédent : 001C18; suivant : 001C20

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Organolithium and organomagnesium compounds of the naphthalene series in organic synthesis

Auteurs :

Source :

• Russian Chemical Reviews [ 0036-021X ] ; 2006-08-31.

RBID : ISTEX:C21D141AB4E77DDB975DABF11CAECADAA373925C

Descripteurs français

• Wicri :
  • topic : Halogène, Magnésium.

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:

• https://api.istex.fr/document/C21D141AB4E77DDB975DABF11CAECADAA373925C/fulltext/pdf

DOI: 10.1070/RC2006v075n08ABEH003611

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