Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Modhu Sudan Maji"'
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 11, Pp o2844-o2844 (2011)
The title compound, C26H18BrNO4, features a functionalized chromene. The cyclohexene ring adopts a sofa conformation and has the nitro group and the bromophenyl ring in an axial position. The ten atoms of the chromene moiety lie close to a common pla
Externí odkaz:
https://doaj.org/article/756065e86ab34c05a67f7018dd88f31a
Publikováno v:
Organic Letters. 24:9001-9006
Benzoperylenocarbazole (BPC), a unique carbazole-based organophotocatalyst, is reported herein as a potent organo-photoreductant. Lower excited state oxidation potential (-2.0 V vs SCE) and reasonable excited state lifetime (4.61 ns) render BPC an ef
Publikováno v:
Handbook of CH-Functionalization. :1-25
Publikováno v:
Angewandte Chemie International Edition.
Publikováno v:
Synthesis.
The chemical diversification of biomolecules set forth a significant area that constitutes an important intersection between chemistry and biology. Amino acids and peptides, are the fundamental building blocks of proteins, play an ubiquitous role in
Publikováno v:
The Journal of Organic Chemistry. 87:4343-4359
Herein, a state-of-the-art one-pot cascade benzannulation technique for the efficacious synthesis of valuable 3-hydroxy-2-methyl carbazoles, a linchpin of more than 25 carbazole-based alkaloids, is unveiled from readily affordable fundamental commodi
Publikováno v:
Organic & Biomolecular Chemistry. 20:3029-3042
The review describes synthesis of functionalized indoles from a pre-existing pyrrole core via cascade benzannulation strategies developed in the last decade. Detailed mechanistic analysis is also discussed to depict the reactivity pattern.
Publikováno v:
Advanced Synthesis & Catalysis. 363:4605-4611
Autor:
Shuvendu Saha, Modhu Sudan Maji
Publikováno v:
Chemical communications (Cambridge, England). 58(77)
Cobalt(iii)-catalyzed thiocarbamate directed aminocarbonylation and amination of C–H bonds are described to access diverse amides.
Publikováno v:
Synthesis. 54:887-909
The oxa-Diels–Alder reaction is a straightforward, atom-economical process for the construction of six-membered oxacycles, which are privileged structures due to their very common occurrence in several pharmaceuticals and natural products. As with