Related Products of 201341-05-1, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 201341-05-1, Name is Tenofovir disoproxil, SMILES is O=C(OC(C)C)OCOP(OCOC(OC(C)C)=O)(CO[C@H](C)CN1C=NC2=C(N)N=CN=C12)=O, belongs to piperidines compound. In a article, author is Grygorenko, Oleksandr O., introduce new discover of the category.
Synthesis of saturated nitrogen heterocycles by Strecker reaction – nucleophilic cyclization
Approaches to alpha-cyanopyrrolidines, -piperidines, and -azepanes, as well as their bi- and polycyclic analogues are surveyed, which are based on Strecker reaction – intramolecular nucleophilic cyclization. The reactions are categorized according to the nature of the internal electrophile participating in the cyclization step, i.e. carboxylic acid or its derivative, carbonyl compound, or alkylating agent. Special attention is paid to one -pot tandem Strecker reaction – S(N)2-type nucleophilic cyclization (STRINC), or cyanide-induced dynamic intramolecular cyclization, which is an efficient and convenient approach to various mono- and bicyclic alpha-amino nitriles and alpha-amino acids. (C) 2020 Elsevier Ltd. All rights reserved.
Related Products of 201341-05-1, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 201341-05-1.
Reference:
Piperidine – Wikipedia,
,Piperidine | C5H11N – PubChem