372199-85-4Relevant articles and documents
A novel approach for substitution of sulfonate group by (1H)-imidazole moiety: An application for synthesis of novel benzyl imidazolylcarbamates
Thripuram, Vijaya Durga,Bollikolla, Hari Babu,Mule, Siva Nagi Reddy,Battula, Sailaja Kumari,Ala, Vasu Babu
, p. 569 - 574 (2018/06/26)
An efficient and convenient substitution protocol was developed for the synthesis of novel benzyl (1-methyl-1H-imidazol-5-yl) (aryl) methyl carbamate derivatives from α-amido sulphones with a solution 5-bromo-1-methyl-(1H)-imidazole in THF under Hexamethy
1-(N -acylamino)alkyl sulfones from N -acyl-α-amino acids or N -alkylamides
Adamek, Jakub,Mazurkiewicz, Roman,Pazdzierniok-Holewa, Agnieszka,Grymel, Miroslawa,Kuznik, Anna,Zielinska, Katarzyna
, p. 2765 - 2770 (2014/04/17)
A variety of N-(1-methoxyalkyl)amides or carbamates react readily with sodium aryl sulfinates in the presence of triphenylphosphonium tetrafluoroborate or bromide in CHCl3 under mild conditions to give 1-(N-acylamino)alkyl sulfones in good yiel
A mild and efficient catalytic mannich-type reaction as a simple access to N -benzyloxycarbonyl -amino ketones
Das, Biswanath,Reddy, Gandolla Chinna,Balasubramanyam, Penagaluri,Veeranjaneyulu, Boyapati
scheme or table, p. 2057 - 2062 (2010/08/13)
N-Benzyloxycarbonylamino sulfones react with aromatic ketones in the presence of catalytic amount of boron trifluoride-diethyl ether at room temperature to afford the corresponding protected β-amino ketones in high yields (71-87%). Georg Thieme Verlag Stu
