3-Azabicyclo[3.3.1]nonane Derivatives: IX. Synthesis and Molecular Structure of 3-Azabicyclo[3.3.1]nonane-1,5-diamines in Solution and in Solid State

Kopyshev, M. V.; Shakhkel'dyan, I. V.; Kozlova, L. М.; Litvin, E. F.; Sharf, V. Z.; Troitskii, N. A.; Atroshchenko, Yu. M.; Alifanova, E. N.; Nikishina, Maria B.; Vorontsov, I. N.; Gurylev, D. V.

doi:10.1023/b:rujo.0000034950.28394.e0

Russian Journal of Organic Chemistry

2004

DOI: 10.1023/b:rujo.0000034950.28394.e0

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3-Azabicyclo[3.3.1]nonane Derivatives: IX. Synthesis and Molecular Structure of 3-Azabicyclo[3.3.1]nonane-1,5-diamines in Solution and in Solid State

M. V. Kopyshev

I. V. Shakhkel'dyan

L. М. Kozlova

et al.

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Cited by 4 publications

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“…The presence of two nitro groups in a molecule of potential biologically active compound could give rise to increased toxicity [4]. 1,5-Dinitro-3-azabicyclo[3.3.1]non-6-enes were previously reduced with molecular hydrogen over nickel or carbon-supported palladium to obtain the corresponding saturated diamines [5] or mixtures of saturated and unsaturated diamines [6]. Taking the above into account, in the present work we made an attempt to find conditions for selective preparation of unsaturated diamines of the 3-azabicyclo[3.3.1]nonane series.…”

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Selective reduction of 6-substituted 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes

Yakunina

Shchukin

Kopyshev³

et al. 2011

Russ J Org Chem

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Selective reduction of 6-substituted 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes

Yakunina

Shchukin

Kopyshev³

et al. 2011

Russ J Org Chem

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3‐Azabicyclo[3.3.1]nonane Derivatives. Part 9. Synthesis and Molecular Structure of 3‐Azabicyclo[3.3.1]nonane‐1,5‐diamines in Solution and in Solid State.

et al. 2004

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Nucleophilic Dearomatizing (D_NAr) Reactions of Aromatic C,H-Systems. A Mature Paradigm in Organic Synthesis

et al. 2007

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Institute fu ¨r Kohlenforschung (Mu ¨lheim a.d. Ruhr) with R. Benn investigating 187 Os NMR. In November 1989 he became Profesor Titular at the University of Oviedo, where he started his own research. He moved to the University of Almerı ´a (1996), where he is Professor of Organic Chemistry. His current research activities range from the application of phosphorus-stabilized carbanions in organic and organometallic chemistry to mechanistic studies of reactions involving organometallic species through multinuclear magnetic resonance. G. Ruiz Go ´mez was born in Madrid, Spain. She studied chemistry at the University of Almerı ´a and completed her first degree (Licenciatura) in July 2000. She was awarded a Ph.D. in 2006 for work on dearomatizing reactions of phosphinamides and phosphonamides under the direction of Professor Lo ´pez Ortiz. She is currently a postdoctoral fellow in Professor Lo ´pez-Ortiz's group with interest in the synthesis of non-natural peptides and peptide analogues.

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3-Azabicyclo[3.3.1]nonane Derivatives: IX. Synthesis and Molecular Structure of 3-Azabicyclo[3.3.1]nonane-1,5-diamines in Solution and in Solid State

Cited by 4 publications

References 2 publications

Selective reduction of 6-substituted 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes

Selective reduction of 6-substituted 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes

3‐Azabicyclo[3.3.1]nonane Derivatives. Part 9. Synthesis and Molecular Structure of 3‐Azabicyclo[3.3.1]nonane‐1,5‐diamines in Solution and in Solid State.

Nucleophilic Dearomatizing (D_NAr) Reactions of Aromatic C,H-Systems. A Mature Paradigm in Organic Synthesis

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3-Azabicyclo[3.3.1]nonane Derivatives: IX. Synthesis and Molecular Structure of 3-Azabicyclo[3.3.1]nonane-1,5-diamines in Solution and in Solid State

Cited by 4 publications

References 2 publications

Selective reduction of 6-substituted 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes

Selective reduction of 6-substituted 1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes

3‐Azabicyclo[3.3.1]nonane Derivatives. Part 9. Synthesis and Molecular Structure of 3‐Azabicyclo[3.3.1]nonane‐1,5‐diamines in Solution and in Solid State.

Nucleophilic Dearomatizing (DNAr) Reactions of Aromatic C,H-Systems. A Mature Paradigm in Organic Synthesis

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Nucleophilic Dearomatizing (D_NAr) Reactions of Aromatic C,H-Systems. A Mature Paradigm in Organic Synthesis