Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Sudipta Mitra"'
Autor:
Sudipta Mitra
Publikováno v:
Indian Journal of Ophthalmology, Vol 71, Iss 5, Pp 2275-2279 (2023)
A woman reported decreased vision in the right eye since hospitalization for COVID-19. Vision in the right eye was 6/18 and in the left eye was counting fingers. Her left eye had cataract and right eye was pseudophakic with earlier documented good re
Externí odkaz:
https://doaj.org/article/9e160bcf503f481f8442ca91f9f826b7
Publikováno v:
The Journal of Physical Chemistry Letters. 14:1892-1898
Autor:
Sudipta Mitra, Anisha Priyadarshi
Publikováno v:
IOSR Journal of Electronics and Communication Engineering. 12:07-12
Publikováno v:
Nordic Pulp & Paper Research Journal. 30:634-639
Publikováno v:
Synthesis. 47:2294-2298
A short and efficient synthetic approach has been developed for the synthesis of a variety of imidazole-fused benzodiazepinones. It is based on a Ugi multicomponent reaction strategy and uses various isocyanides to generate the key intermediates for
Publikováno v:
RSC Adv.. 3:1862-1870
A short and efficient synthetic route to novel benzimidazo[1,2-d]dibenzo[b,f][1,4]diazepines has been developed using a copper catalyzed intramolecular Ullmann type C–N bond forming reaction as a key step. Copper iodide and 1,10-phenanthroline furn
Publikováno v:
Synthesis. 45:85-92
An efficient three-step synthetic route to imidazole-fused benzodiazepines from imidazole-2-carbaldehyde is described. Application of intramolecular Buchwald–Hartwig cycloamination reaction in the final step is shown to be a convenient method for t
Publikováno v:
ChemInform. 46
Ugi three-component reaction generates key intermediates for a Mumm rearrangement to form the title compounds (IV).
Publikováno v:
Synthesis. 2010:3899-3905
An efficient one-pot reaction between isocyanides, anilines, and salicylaldehydes (2-hydroxybenzaldehydes) in the presence of a Lewis acid proceeds smoothly at room temperature within a short time interval to afford aminobenzofurans and Nalkyl- 2-ary
Publikováno v:
ChemInform. 44
The intramolecular Buchwald—Hartwig cycloamination reaction of precursors (V) is the key-step in the three-step synthetic route to the title benzodiazepines (VI).