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Challenges in the development of organic and hybrid molecular systems

Konstantin Igorevich Galkin 1
Konstantin Igorevich Galkin
Mikhail Petrovich Egorov 1
Mikhail Petrovich Egorov
Alexey Mikhailovich Sakharov 1
Alexey Mikhailovich Sakharov
Sergei Grigorievich Zlotin 1
Sergei Grigorievich Zlotin
Elena Andreevna Redina 1
Elena Andreevna Redina
Vera I Isaeva 1
Vera I Isaeva
Marina Leonidovna Gening 1
Marina Leonidovna Gening
Nikolay Eduardovich Nifantiev 1
Nikolay Eduardovich Nifantiev
Published 2016-09-08
Focus articleVolume 26, Issue 5, 365-374
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Ananikov V. P. et al. Challenges in the development of organic and hybrid molecular systems // Mendeleev Communications. 2016. Vol. 26. No. 5. pp. 365-374.
GOST all authors (up to 50) Copy
Ananikov V. P., Galkin K. I., Egorov M. P., Sakharov A. M., Zlotin S. G., Redina E. A., Isaeva V. I., Kustov L. M., Gening M. L., Nifantiev N. E. Challenges in the development of organic and hybrid molecular systems // Mendeleev Communications. 2016. Vol. 26. No. 5. pp. 365-374.
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TY - JOUR
DO - 10.1016/j.mencom.2016.09.001
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.09.001
TI - Challenges in the development of organic and hybrid molecular systems
T2 - Mendeleev Communications
AU - Ananikov, Valentin Pavlovich
AU - Galkin, Konstantin Igorevich
AU - Egorov, Mikhail Petrovich
AU - Sakharov, Alexey Mikhailovich
AU - Zlotin, Sergei Grigorievich
AU - Redina, Elena Andreevna
AU - Isaeva, Vera I
AU - Kustov, Leonid Modestovich
AU - Gening, Marina Leonidovna
AU - Nifantiev, Nikolay Eduardovich
PY - 2016
DA - 2016/09/08
PB - Mendeleev Communications
SP - 365-374
IS - 5
VL - 26
ER -
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@article{2016_Ananikov,
author = {Valentin Pavlovich Ananikov and Konstantin Igorevich Galkin and Mikhail Petrovich Egorov and Alexey Mikhailovich Sakharov and Sergei Grigorievich Zlotin and Elena Andreevna Redina and Vera I Isaeva and Leonid Modestovich Kustov and Marina Leonidovna Gening and Nikolay Eduardovich Nifantiev},
title = {Challenges in the development of organic and hybrid molecular systems},
journal = {Mendeleev Communications},
year = {2016},
volume = {26},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.09.001},
number = {5},
pages = {365--374},
doi = {10.1016/j.mencom.2016.09.001}
}
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Ananikov, Valentin Pavlovich, et al. “Challenges in the development of organic and hybrid molecular systems.” Mendeleev Communications, vol. 26, no. 5, Sep. 2016, pp. 365-374. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.09.001.
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Abstract

The rapid development of organic chemistry and catalysis has provided outstanding chemical tools to build complex molecular architectures that were never possible before. In spite of amazing progress in studying individual molecules and reactions, practical applications are limited due to the high cost of newly developed technologies and the difficulty in understanding the processes at the molecular level. Herein, we summarize our first steps and experiences carrying out an ongoing project on organic and hybrid molecular systems that highlights new fascinating opportunities and identifies future challenges.

References

1.
Reinventing Chemistry
Whitesides G.M.
Angewandte Chemie - International Edition, 2015
3.
Contemporary screening approaches to reaction discovery and development.
Collins K.D., Gensch T., Glorius F.
Nature Chemistry, 2014
4.
Nanotools for neuroscience and brain activity mapping.
Alivisatos A.P., Andrews A.M., Boyden E.S., Chun M., Church G.M., Deisseroth K., Donoghue J.P., Fraser S.E., Lippincott-Schwartz J., Looger L.L., Masmanidis S., McEuen P.L., Nurmikko A.V., Park H., Peterka D.S., et. al.
ACS Nano, 2013
5.
The Brain Activity Map
Alivisatos A.P., Chun M., Church G.M., Deisseroth K., Donoghue J.P., Greenspan R.J., McEuen P.L., Roukes M.L., Sejnowski T.J., Weiss P.S., Yuste R.
Science, 2013
6.
Microfluidics: A new cosset for neurobiology
Wang J., Ren L., Li L., Liu W., Zhou J., Yu W., Tong D., Chen S.
Lab on a Chip, 2009
7.
Nano-Bioelectronics
Zhang A., Lieber C.M.
Chemical Reviews, 2015
8.
Gene-targeted microfluidic cultivation validated by isolation of a gut bacterium listed in Human Microbiome Project's Most Wanted taxa
Ma L., Kim J., Hatzenpichler R., Karymov M.A., Hubert N., Hanan I.M., Chang E.B., Ismagilov R.F.
Proceedings of the National Academy of Sciences of the United States of America, 2014
9.
Indigenous Bacteria from the Gut Microbiota Regulate Host Serotonin Biosynthesis
Yano J., Yu K., Donaldson G., Shastri G., Ann P., Ma L., Nagler C., Ismagilov R., Mazmanian S., Hsiao E.
Cell, 2015
10.
Modern organic synthesis
Egorov M.P.
Russian Chemical Reviews, 2014
11.
Development of new methods in modern selective organic synthesis: Preparation of functionalized molecules with atomic precision
Ananikov V.P., Khemchyan L.L., Ivanova Y.V., Bukhtiyarov V.I., Sorokin A.M., Prosvirin I.P., Vatsadze S.Z., Medved'ko A.V., Nuriev V.N., Dilman A.D., Levin V.V., Koptyug I.V., Kovtunov K.V., Zhivonitko V.V., Likholobov V.A., et. al.
Russian Chemical Reviews, 2014
12.
Catalysis to Build Molecular Complexity with Atomic Precision
Ananikov V., Liu X., Schneider U.
Chemistry - An Asian Journal, 2016
15.
Target-oriented analysis of gaseous, liquid and solid chemical systems by mass spectrometry, nuclear magnetic resonance spectroscopy and electron microscopy
Kachala V.V., Khemchyan L.L., Kashin A.S., Orlov N.V., Grachev A.A., Zalesskiy S.S., Ananikov V.P.
Russian Chemical Reviews, 2013
16.
Ananikov V.P., Khokhlova E.A., Egorov M.P., Sakharov A.M., Zlotin S.G., Kucherov A.V., Kustov L.M., Gening M.L., Nifantiev N.E.
Mendeleev Communications, 2015
17.
10.1016/j.mencom.2016.09.001_sbref0055a
Anastas
Green Chemistry: Theory and Practice, 1998
18.
10.1016/j.mencom.2016.09.001_sbref0055b
Handbook of Green Chemistry and Technology, 2002
20.
Progress in 1,2,3,4-Tetrazine Chemistry
Churakov A.M., Tartakovsky V.A.
Chemical Reviews, 2004
21.
Are DTTO and iso -DTTO Worthwhile Targets for Synthesis?
Christe K.O., Dixon D.A., Vasiliu M., Wagner R.I., Haiges R., Boatz J.A., Ammon T.L.
Propellants, Explosives, Pyrotechnics, 2015
22.
10.1016/j.mencom.2016.09.001_sbref0065b
Jorgensen
Mater., 2011
23.
10.1016/j.mencom.2016.09.001_sbref0065c
Politzer
Cent. Eur. J. Energ. Mater., 2013
25.
Nucleophilic substitution in benzo-1,2,3,4-tetrazine 1,3-dioxides
Smirnov O.Y., Churakov A.M., Tyurin A.Y., Strelenko Y.A., Ioffe S.L., Tartakovsky V.A.
Russian Chemical Bulletin, 2002
26.
Ozonation of benzotetrazine 1,3-dioxides. Facile synthesis of di(methoxycarbonyl)-1,2,3,4-tetrazine 1,3-dioxide
Klenov M.S., Churakov A.M., Strelenko Y.A., Ananyev I.V., Lyssenko K.A., Tartakovsky V.A.
Tetrahedron Letters, 2015
27.
Toward the Synthesis of Tetrazino-­tetrazine 1,3,6,8-Tetraoxide (TTTO): An Approach to Non-annulated 1,2,3,4-Tetrazine 1,3-Dioxides
Klenov M.S., Anikin O.V., Churakov A.M., Strelenko Y.A., Fedyanin I.V., Ananyev I.V., Tartakovsky V.A.
European Journal of Organic Chemistry, 2015
28.
Zlotin S.G., Churakov A.M., Luk’yanov O.A., Makhova N.N., Sukhorukov A.Y., Tartakovsky V.A.
Mendeleev Communications, 2015
29.
Cascade Reactions in Total Synthesis
Nicolaou K.C., Edmonds D.J., Bulger P.G.
Angewandte Chemie - International Edition, 2006
30.
10.1016/j.mencom.2016.09.001_sbref0100a
Multicomponent Reactions, 2005
31.
10.1016/j.mencom.2016.09.001_sbref0100b
Synthesis of Heterocycles via Multicomponent Reactions I, 2010
32.
Vereshchagin A.N., Elinson M.N., Anisina Y.E., Ryzhkov F.V., Goloveshkin A.S., Bushmarinov I.S., Zlotin S.G., Egorov M.P.
Mendeleev Communications, 2015
33.
Aminocyanopyridine inhibitors of mitogen activated protein kinase-activated protein kinase 2 (MK-2)
Anderson D.R., Hegde S., Reinhard E., Gomez L., Vernier W.F., Lee L., Liu S., Sambandam A., Snider P.A., Masih L.
Bioorganic and Medicinal Chemistry Letters, 2005
34.
10.1016/j.mencom.2016.09.001_sbref0115a
2012
35.
10.1016/j.mencom.2016.09.001_sbref0115b
2013
36.
Recent Advances in Organocatalytic Methods for Asymmetric CC Bond Formation
37.
Asymmetric organocatalysis: from proline to highly efficient immobilized organocatalysts
Kucherenko A.S., Siyutkin D.E., Maltsev O.V., Kochetkov S.V., Zlotin S.G.
Russian Chemical Bulletin, 2012
40.
A convenient enantioselective decarboxylative aldol reaction to access chiral α-hydroxy esters using β-keto acids
Duan Z., Han J., Qian P., Zhang Z., Wang Y., Pan Y.
Beilstein Journal of Organic Chemistry, 2014
42.
Recent Developments in Asymmetric Organocatalytic Domino Reactions
43.
Enantioselective Organocatalyzed Domino Synthesis of Six-Membered Carbocycles
Rodriguez J., Bonne D., Goudedranche S., Raimondi W., Bugaut X., Constantieux T.
Synthesis, 2013
45.
Bifunctional Amine-Squaramides: Powerful Hydrogen-Bonding Organocatalysts for Asymmetric Domino/Cascade Reactions
Chauhan P., Mahajan S., Kaya U., Hack D., Enders D.
Advanced Synthesis and Catalysis, 2015
46.
10.1016/j.mencom.2016.09.001_bib0145
Kerton
Alternative Solvents for Green Chemistry, 2010
47.
10.1016/j.mencom.2016.09.001_sbref0150a
Leitner
2010
52.
Asymmetric catalytic synthesis of functionalized tetrahydroquinolines in supercritical fluids
Filatova E.V., Turova O.V., Kuchurov I.V., Kostenko A.A., Nigmatov A.G., Zlotin S.G.
Journal of Supercritical Fluids, 2016
53.
Antiplasmodial and Cytotoxic Activity of Galipinine and other Tetrahydroquinolines from Galipea officinalis
Jacquemond-Collet I., Benoit-Vical F., Valentin A., Stanislas E., Mallié M., Fourasté I.
Planta Medica, 2002
54.
Two tetrahydroquinoline alkaloids from Galipea officinalis
JACQUEMONDCOLLET I., HANNEDOUCHE S., FABRE N., FOURASTE I., MOULIS C.
Phytochemistry, 1999
55.
Martinelline and Martinellic Acid, Novel G-Protein Linked Receptor Antagonists from the Tropical Plant Martinella iquitosensis (Bignoniaceae)
Witherup K.M., Ransom R.W., Graham A.C., Bernard A.M., Salvatore M.J., Lumma W.C., Anderson P.S., Pitzenberger S.M., Varga S.L.
Journal of the American Chemical Society, 1995
57.
Applications of asymmetric organocatalysis in medicinal chemistry
Alemán J., Cabrera S.
Chemical Society Reviews, 2013
59.
From carbohydrate leads to glycomimetic drugs
Ernst B., Magnani J.L.
Nature Reviews Drug Discovery, 2009
60.
Recent Developments in Synthetic Carbohydrate-Based Diagnostics, Vaccines, and Therapeutics.
Fernández-Tejada A., Cañada F.J., Jiménez-Barbero J.
Chemistry - A European Journal, 2015
61.
Glycans in Medicinal Chemistry: An Underexploited Resource
Fernández-Tejada A., Cañada F.J., Jiménez-Barbero J.
ChemMedChem, 2015
62.
10.1016/j.mencom.2016.09.001_bib0200
Ustyuzhanina
Synlett., 2006
63.
Design of α-Selective Glycopyranosyl Donors Relying on Remote Anchimeric Assistance
Komarova B.S., Tsvetkov Y.E., Nifantiev N.E.
Chemical Record, 2016
64.
10.1016/j.mencom.2016.09.001_bib0370
Komarova
2016
65.
Synthesis of a Pentasaccharide and Neoglycoconjugates Related to Fungal α-(1→3)-Glucan and Their Use in the Generation of Antibodies to TraceAspergillus fumigatusCell Wall
Komarova B.S., Orekhova M.V., Tsvetkov Y.E., Beau R., Aimanianda V., Latgé J., Nifantiev N.E.
Chemistry - A European Journal, 2014
66.
A Blockwise Approach to the Synthesis of (1→2)-Linked Oligosac­char­ides Corresponding to Fragments of the Acid-Stable β-Mannan from theCandida albicansCell Wall
Karelin A.A., Tsvetkov Y.E., Paulovičová E., Paulovičová L., Nifantiev N.E.
European Journal of Organic Chemistry, 2016
67.
Homogeneous azidophenylselenylation of glycals using TMSN3–Ph2Se2–PhI(OAc)2
Mironov Y.V., Sherman A.A., Nifantiev N.E.
Tetrahedron Letters, 2004
69.
Pyridine Nucleosides Neopetrosides A and B from a Marine Neopetrosia sp. Sponge. Synthesis of Neopetroside A and Its β-Riboside Analogue
Shubina L.K., Makarieva T.N., Yashunsky D.V., Nifantiev N.E., Denisenko V.A., Dmitrenok P.S., Dyshlovoy S.A., Fedorov S.N., Krasokhin V.B., Jeong S.H., Han J., Stonik V.A.
Journal of Natural Products, 2015
70.
Synthesis and Biological Evaluation of Cyanogenic Glycosides
Yashunsky D.V., Kulakovskaya E.V., Kulakovskaya T.V., Zhukova O.S., Kiselevskiy M.V., Nifantiev N.E.
Journal of Carbohydrate Chemistry, 2015
71.
The role of serum carcinoembryonic antigen in predicting responses to chemotherapy and survival in patients with non-small cell lung cancer
Song Y., Liu H., Gu X., Lv T., Li Y., Wu Y., Xiao Y., Yuan D.
Journal of Cancer Research and Therapeutics, 2014
73.
Synthesis, NMR, and Conformational Studies of Cyclic Oligo-(1→6)-β-D-Glucosamines
Gening M.L., Titov D.V., Grachev A.A., Gerbst A.G., Yudina O.N., Shashkov A.S., Chizhov A.O., Tsvetkov Y.E., Nifantiev N.E.
European Journal of Organic Chemistry, 2010
74.
Synthesis of Multivalent Carbohydrate-Centered Glycoclusters as Nanomolar Ligands of the Bacterial Lectin LecA from Pseudomonas aeruginosa
Gening M.L., Titov D.V., Cecioni S., Audfray A., Gerbst A.G., Tsvetkov Y.E., Krylov V.B., Imberty A., Nifantiev N.E., Vidal S.
Chemistry - A European Journal, 2013
75.
Cyclo-oligo-(1 → 6)-β-d-glucosamine based artificial channels for tunable transmembrane ion transport
Saha T., Roy A., Gening M.L., Titov D.V., Gerbst A.G., Tsvetkov Y.E., Nifantiev N.E., Talukdar P.
Chemical Communications, 2014
76.
Trimodal Control of Ion-Transport Activity on Cyclo-oligo-(1→6)-β-D-glucosamine-Based Artificial Ion-Transport Systems
Roy A., Saha T., Gening M.L., Titov D.V., Gerbst A.G., Tsvetkov Y.E., Nifantiev N.E., Talukdar P.
Chemistry - A European Journal, 2015
77.
Hopping-Mediated Anion Transport through a Mannitol-Based Rosette Ion Channel
Saha T., Dasari S., Tewari D., Prathap A., Sureshan K.M., Bera A.K., Mukherjee A., Talukdar P.
Journal of the American Chemical Society, 2014
84.
Industrial applications of metal–organic frameworks
Czaja A.U., Trukhan N., Müller U.
Chemical Society Reviews, 2009
85.
A Chromium Terephthalate-Based Solid with Unusually Large Pore Volumes and Surface Area
Férey G., Mellot-Draznieks C., Serre C., Millange F., Dutour J., Surblé S., Margiolaki I.
Science, 2005
88.
10.1016/j.mencom.2016.09.001_bib0325
Lin
Appl. Catal. A: General, 2012
89.
Isaeva V.I., Tarasov A.L., Chernyshev V.V., Kustov L.M.
Mendeleev Communications, 2015
90.
A Chemically Functionalizable Nanoporous Material [Cu3(TMA)2(H2O)3]n
Chui S.S., Lo S.M., Charmant J.P., Orpen A.G., Williams I.D.
Science, 1999
91.
Exceptional chemical and thermal stability of zeolitic imidazolate frameworks
Park K.S., Ni Z., Côté A.P., Choi J.Y., Huang R., Uribe-Romo F.J., Chae H.K., O’Keeffe M., Yaghi O.M.
Proceedings of the National Academy of Sciences of the United States of America, 2006
92.
In situ synthesis of novel ZIF-8 membranes on polymeric and inorganic supports
Isaeva V.I., Barkova M.I., Kustov L.M., Syrtsova D.A., Efimova E.A., Teplyakov V.V.
Journal of Materials Chemistry A, 2015
93.
Preparation of bimetallic gold catalysts by redox reaction on oxide-supported metals for green chemistry applications
Redina E.A., Kirichenko O.A., Greish A.A., Kucherov A.V., Tkachenko O.P., Kapustin G.I., Mishin I.V., Kustov L.M.
Catalysis Today, 2015
97.
Critical Influence of 5-Hydroxymethylfurfural Aging and Decomposition on the Utility of Biomass Conversion in Organic Synthesis.
Galkin K.I., Krivodaeva E.A., Romashov L.V., Zalesskiy S.S., Kachala V.V., Burykina J.V., Ananikov V.P.
Angewandte Chemie - International Edition, 2016
105.
10.1016/j.mencom.2016.09.001_bib0365
Bauer
Nat. Mater., 2016