Abstract:
Each great discovery is inexhaustible as science itself, and is strictly addressed to those who did found his or her predestination for trying to understand it and to develop it. What was a basis for the Pasteur discovery, what is the essence of it, and what kind of consequences have been found from it, all these points are considered in this paper.
Document Type:
Article
Language: English
Citation:
R. G. Kostyanovsky, “Louis Pasteur did it for us especially”, Mendeleev Commun., 13:3 (2003), 85–90
Linking options:
https://www.mathnet.ru/eng/mendc3969
https://www.mathnet.ru/eng/mendc/v13/i3/p85
This publication is cited in the following 17 articles:
Hasnain Sajid, Tariq Mahmood, Muhammad Sohaib, Khurshid Ayub, Adnan Younis, Ali S. Alshomrany, Muhammad Imran, “Solvent efficiency and role of dispersion and electrostatic forces for chiral discrimination of sulfur-containing amino acids by tetra-protonated CBPQT macrocycle”, Journal of Molecular Liquids, 399 (2024), 124384
Areeg Sajjad, Sehrish Sarfaraz, Khurshid Ayub, “Chiral Discrimination of Amino Acids by Using a Twisted Carbon Nanobelt: A DFT Study”, ACS Appl. Nano Mater., 7:15 (2024), 18065
Maria Asghar, Ahmed Lakhani, Misbah Asif, Nadeem S. Sheikh, Muhammad Ali Hashmi, Ralf Ludwig, Hassan H. Hammud, Khurshid Ayub, “Chiral Recognition of Amino Acids Using CC2 Porous Organic Cages”, J. Phys. Chem. A, 127:19 (2023), 4245
Kinga Roszak, Andrzej Katrusiak, “High-Pressure Crystallization and Thermodynamic Stability Study on the Resolution of High-Density Enantiomers from Low-Density Racemates”, Org. Lett., 25:1 (2023), 37
Gourav M. Upadhyay, Hemant M. Mande, Dhruvi K. Pithadia, Ronak H. Maradiya, Ashutosh V. Bedekar, “Effect of the Position of the Cyano Group on Molecular Recognition, Supramolecular Superhelix Architecture, and Spontaneous Resolution of Aza[7]helicenes”, Crystal Growth & Design, 19:9 (2019), 5354
Karl‐Heinz Ernst, Surface and Interface Science, 2016, 695
Rakesh Puttreddy, James A. Hutchison, Yuri Gorodetski, Jack Harrowfield, Kari Rissanen, “Enantiomer Separation of Tris(2,2′-bipyridine)ruthenium(II): Interaction of aD3-Symmetric Cation with aC2-Symmetric Anion”, Crystal Growth & Design, 15:4 (2015), 1559
Jan Vávra, Lukáš Severa, Ivana Císařová, Blanka Klepetářová, David Šaman, Dušan Koval, Václav Kašička, Filip Teplý, “Search for Conglomerate in Set of [7]Helquat Salts: Multigram Resolution of Helicene–Viologen Hybrid by Preferential Crystallization”, J. Org. Chem., 78:4 (2013), 1329
Michiya Fujiki, “Mirror symmetry breaking of silicon polymers—from weak bosons to artificial helix”, The Chemical Record, 9:5 (2009), 271
Gérard Coquerel, David B. Amabilino, Chirality at the Nanoscale, 2009, 305
David B. Amabilino, “How Deformation Can Lend a Hand to Molecular Ordering”, Science, 325:5939 (2009), 402
David B. Amabilino, “Chiral nanoscale systems: preparation, structure, properties and function”, Chem. Soc. Rev., 38:3 (2009), 669
Joseph Gal, “When did Louis Pasteur present his memoir on the discovery of molecular chirality to the Académie des sciences? Analysis of a discrepancy”, Chirality, 20:10 (2008), 1072
Witold K. Rybak, “Asymmetric autocatalysis: crystallization-induced highly enantioselective synthesis of a conglomerating oxo-rhenium(V) complex”, Tetrahedron: Asymmetry, 19:19 (2008), 2234
Lluïsa Pérez-García, David B. Amabilino, “Spontaneous resolution, whence and whither: from enantiomorphic solids to chiral liquid crystals, monolayers and macro- and supra-molecular polymers and assemblies”, Chem. Soc. Rev., 36:6 (2007), 941
R. G. Kostyanovsky, “Impossible things in stereochemistry”, Mendeleev Commun., 14:6 (2004), 229–230