Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mattijs Baeten"'
Autor:
Jennifer Albaneze-Walker, Gregor Urbanietz, Andras Horvath, Stefano Lancianesi, Alejandro Gimenez Molina, Thomas De Vijlder, Mattijs Baeten, Martine Canters
Publikováno v:
The Journal of organic chemistry. 87(19)
Azido nucleosides couple with phosphoramidites via an initial iminophosphorane, which eliminates acrylonitrile to generate the coupled dimer P(V) product. The vulnerable phosphite triester intermediate is bypassed entirely, making the methodology ver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ca3f94cb9f0cdeeabe6514bfa045fa6
https://pubmed.ncbi.nlm.nih.gov/36161801
https://pubmed.ncbi.nlm.nih.gov/36161801
Publikováno v:
Analytical Science Advances. 2:109-127
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f71cc2009f232db59d3f4653b1f5de4
https://doi.org/10.1002/ansa.202000155
https://doi.org/10.1002/ansa.202000155
Publikováno v:
Advanced synthesis and catalysis
In this work an efficient tandem process transforming N-substituted amidines into secondary amides has been described. The process involves N-acylurea formation by reaction of the substrate with bis(acyloxy)(phenyl)-λ3-iodane followed by isocyanate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1aeba42f36d8c777a35670170753860c
https://doi.org/10.1002/adsc.201400648
https://doi.org/10.1002/adsc.201400648
Autor:
Bert U. W. Maes, Mattijs Baeten
There are many methods available in the synthetic toolbox to construct carbon–nitrogen bonds, but these standardly require preactivation of the substrate. These involve classical, nonmetal catalyzed methods (e.g., nucleophilic substitutions) and ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::938075687ed383a7a540d7d1196c66a2
https://doi.org/10.1016/bs.adomc.2017.04.003
https://doi.org/10.1016/bs.adomc.2017.04.003
Autor:
Mattijs Baeten, Bert U. W. Maes
Publikováno v:
ChemInform. 47
A general method for transformation of readily available, stable amidine substrates into substituted guanidines is developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::417b6889f5f26e105ffd2c2948133ab6
https://doi.org/10.1002/chin.201628080
https://doi.org/10.1002/chin.201628080
Autor:
Bert U. W. Maes, Mattijs Baeten
Publikováno v:
Advanced synthesis and catalysis
The use of amidines for the tandem or one-pot synthesis of guanidines is reported. Guanidines are obtained by oxidative rearrangement of readily available and stable amidines into carbodiimides, followed by in situ reaction with amines. The protocol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf4d099f37f6deaeaf292fde1dc21d6a
https://hdl.handle.net/10067/1307260151162165141
https://hdl.handle.net/10067/1307260151162165141
Publikováno v:
The journal of organic chemistry
The potential of halogen−magnesium exchange reactions, followed by quenching with electrophiles, for the functionalization of the pyridazin-3(2H)-one core was investigated. 2-Benzyl-4-bromo-5-methoxy- (1), 2-benzyl-5-bromo-4-methoxy- (4), and 2-ben
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e9527bdef1e98ecab3eff21447a603d
https://doi.org/10.1021/jo9020985
https://doi.org/10.1021/jo9020985
Publikováno v:
ChemInform. 46
This new, efficient tandem process for the transformation of N-substituted amidines into secondary amides is applicable for aliphatic and (hetero)aromatic compounds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8d8a4db4bbeeca5ac9aeab8072af79e
https://doi.org/10.1002/chin.201522102
https://doi.org/10.1002/chin.201522102
Publikováno v:
ChemInform. 41
The potential of halogen−magnesium exchange reactions, followed by quenching with electrophiles, for the functionalization of the pyridazin-3(2H)-one core was investigated. 2-Benzyl-4-bromo-5-methoxy- (1), 2-benzyl-5-bromo-4-methoxy- (4), and 2-ben
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49c7b1f3fb2b3343078261b1b2bf2054
https://doi.org/10.1002/chin.201017160
https://doi.org/10.1002/chin.201017160