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Thermochemistry of hydrogen bonding of proton acceptors in the media of linear and cyclic amides. Cooperativity effects in multi-particle complexes of amides acceptors (B) in the medium of linear (N-methylformamide (NMF)) and cyclic (2-pyrrolidone (Py)) amides
Ruthenium-Catalyzed Reductive Amidation without an External Hydrogen SourceA catalytic reaction between aldehydes and primary amides that leads to N-alkylated amides
Propargyl-Assisted Selective Amidation Applied in C-terminal Glycine Peptide Conjugation-withdrawing inductive effects. Based on this concept of propargyl-assisted selective amidation, a direct application
Thermochemistry of hydrogen bonding of proton acceptors in the media of linear and cyclic amides. Cooperativity effects in multi-particle complexes of amides acceptors (B) in the medium of linear (N-methylformamide (NMF)) and cyclic (2-pyrrolidone (Py)) amides
THE CYCLICITY OF THE DEVELOPMENT OF THE GLOBAL ECONOMIC SYSTEM AMID PRESENT-DAY GLOBALIZATIONTHE CYCLICITY OF THE DEVELOPMENT OF THE GLOBAL ECONOMIC SYSTEM AMID PRESENT-DAY GLOBALIZATION
The Cyclicity of the Development of the Global Economic System amid Present - Day GlobalizationThe Cyclicity of the Development of the Global Economic System amid Present - Day Globalization
Propargyl-Assisted Selective Amidation Applied in C-terminal Glycine Peptide Conjugation-withdrawing inductive effects. Based on this concept of propargyl-assisted selective amidation, a direct application
Thermochemistry of solution, solvation, and hydrogen bonding of cyclic amides in proton acceptor and donor solvents. Amide cycle size effect amides in proton acceptor (B) and proton donor (RXH) solvents were studied. The infinite dilution
Synthesis of stereoisomers of ρ-teft-butylthiacalix[4]arenes tetrasubstituted at the lower rim containing secondary amide groups and their complexation with a number of singly charged anions at the lower rim and containing secondary amide groups to form complexes with a number of spherical (F-, Cl
Thermochemistry of hydrogen bonding of linear and cyclic amides in proton acceptors media (АА), N-methylacetamide (NMA), N,N-dimethylacetamide (DMAA)) and cyclic amides (2-pyrrolidone (Py), N
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