Reactivity of phosphacarbamates: transfer of the carbamate group promoted by metal-assisted electrophilic attack at the carbon dioxide moiety

Michele Aresta; Eugenio Quaranta

doi:10.1021/jo00252a066

Reactivity of phosphacarbamates: transfer of the carbamate group promoted by metal-assisted electrophilic attack at the carbon dioxide moiety

The Journal of Organic Chemistry ◽

10.1021/jo00252a066 ◽

1988 ◽

Vol 53 (17) ◽

pp. 4153-4154 ◽

Cited By ~ 27

Author(s):

Michele Aresta ◽

Eugenio Quaranta

Keyword(s):

Carbon Dioxide ◽

Electrophilic Attack ◽

Carbamate Group

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ChemInform Abstract: Reactivity of Phosphacarbamates: Transfer of the Carbamate Group Promoted by Metal Assisted Electrophilic Attack at the Carbon Dioxide Moiety.

ChemInform ◽

10.1002/chin.198905218 ◽

1989 ◽

Vol 20 (5) ◽

Author(s):

M. ARESTA ◽

E. QUARANTA

Keyword(s):

Carbon Dioxide ◽

Electrophilic Attack ◽

Carbamate Group

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ChemInform Abstract: Carbon Dioxide: A Reagent for Simultaneous Protection of Nucleophilic Centers and the Activation of Alternative Locations to Electrophilic Attack. Part 10. α-Metalation of Tetrahydroquinoline and Indoline via Their Lithium Carbamates:

ChemInform ◽

10.1002/chin.198918217 ◽

1989 ◽

Vol 20 (18) ◽

Author(s):

A. R. KATRITZKY ◽

S. SENGUPTA

Keyword(s):

Carbon Dioxide ◽

Electrophilic Attack

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ChemInform Abstract: Carbon Dioxide: A Reagent for the Protection of Nucleophilic Centres and the Simultaneous Activation of Electrophilic Attack.

Chemischer Informationsdienst ◽

10.1002/chin.198637211 ◽

1986 ◽

Vol 17 (37) ◽

Author(s):

A. R. KATRITZKY ◽

K. AKUTAGAWA

Keyword(s):

Carbon Dioxide ◽

Electrophilic Attack ◽

Simultaneous Activation

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Carbon dioxide: a reagent for the simultaneous protection of nucleophilic centers and the activation of alternative locations to electrophilic attack. 17. Substitution of N-methyl-1- and N-methyl-2-naphthylamine and side-chain functionalization of o-toluidine

The Journal of Organic Chemistry ◽

10.1021/jo00017a012 ◽

1991 ◽

Vol 56 (17) ◽

pp. 5045-5048 ◽

Cited By ~ 20

Author(s):

Alan R. Katritzky ◽

Michael Black ◽

Wei Qiang Fan

Keyword(s):

Carbon Dioxide ◽

Side Chain ◽

Electrophilic Attack

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Carbon Dioxide: A Peagent for the Protection of Nucleophilic Centres and the Simultaneous Activation to Electrophilic Attack-Part Xii. One-Pot Conversion of 3-Methylindole into 2-Formyl-3-Methylindole

Synthetic Communications ◽

10.1080/00397918808060902 ◽

1988 ◽

Vol 18 (10) ◽

pp. 1151-1158 ◽

Cited By ~ 16

Author(s):

Alan R. Katritzky ◽

Kunihiko Akutagawa ◽

R. Alan Jones

Keyword(s):

Carbon Dioxide ◽

Electrophilic Attack ◽

One Pot ◽

Simultaneous Activation

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Carbon dioxide: a reagent for the simultaneous protection of nucleophilic centres and the activation of alternative locations to electrophilic attack

Tetrahedron ◽

10.1016/s0040-4020(01)86820-4 ◽

1987 ◽

Vol 43 (10) ◽

pp. 2343-2348 ◽

Cited By ~ 14

Author(s):

Alan R. Katritzky ◽

Wei-Qiang Fan ◽

Anna E. Koziol ◽

Gus J. Palenik

Keyword(s):

Carbon Dioxide ◽

Electrophilic Attack

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ChemInform Abstract: Carbon Dioxide: A Reagent for Protection of the Nucleophilic Centers and the Simultaneous Activation of Alternative Locations to Electrophilic Attack. Part 13. A New Synthetic Method for the 2-Substitution of Pyrrole.

ChemInform ◽

10.1002/chin.198924156 ◽

1989 ◽

Vol 20 (24) ◽

Author(s):

A. R. KATRITZKY ◽

K. AKUTAGAWA

Keyword(s):

Carbon Dioxide ◽

Synthetic Method ◽

Electrophilic Attack ◽

Simultaneous Activation

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Carbon dioxide: a reagent for simultaneous protection of nucleophilic centers and the activation of alternative locations to electrophilic attack. V. Activation of the 2-alkyl group of a 2-alkylindole toward proton loss and subsequent electrophilic substitution

Journal of the American Chemical Society ◽

10.1021/ja00281a061 ◽

1986 ◽

Vol 108 (21) ◽

pp. 6808-6809 ◽

Cited By ~ 43

Author(s):

Alan R. Katritzky ◽

Kunihiko. Akutagawa

Keyword(s):

Carbon Dioxide ◽

Alkyl Group ◽

Electrophilic Substitution ◽

Electrophilic Attack ◽

Proton Loss

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ChemInform Abstract: Carbon Dioxide: A Reagent for the Simultaneous Protection of Nucleophilic Centres and the Activation of Alternative Locations to Electrophilic Attack. Part 8. A Novel Synthetic Route to 4-Substituted 2-Pyridones.

ChemInform ◽

10.1002/chin.198740185 ◽

1987 ◽

Vol 18 (40) ◽

Author(s):

A. R. KATRITZKY ◽

W.-Q. FAN ◽

A. E. KOZIOL ◽

G. J. PALENIK

Keyword(s):

Carbon Dioxide ◽

Synthetic Route ◽

Electrophilic Attack

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ChemInform Abstract: Carbon Dioxide: A Reagent for the Simultaneous Protection of Nucleophilic Centers and the Activation of Alternative Locations to Electrophilic Attack. Part 16. A Novel Synthetic Method for the Side-Chain Functionalization of N-Methyl-

ChemInform ◽

10.1002/chin.199034108 ◽

1990 ◽

Vol 21 (34) ◽

Author(s):

A. R. KATRITZKY ◽

W.-Q. FAN ◽

K. AKUTAGAWA ◽

J. WANG

Keyword(s):

Carbon Dioxide ◽

Side Chain ◽

Synthetic Method ◽

Electrophilic Attack

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