Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Soham Maity"'
Autor:
Soham Maity, Courtney Bingham, Wei Sheng, Nona Ehyaei, Debarshi Chakraborty, Setare Tahmasebi-Nick, Thomas E. Kimmel, Chrysoula Vasileiou, James H. Geiger, Babak Borhan
Publikováno v:
The Analyst. 148:1085-1092
An engineered hCRBPII protein binds a coumarin-based fluorophore to yield a photoswitchable system via Michael/retro-Michael addition of a cysteine residue. Alternate UV/visible light irradiation accesses the two optical states.
Autor:
James E. Jackson, Piotr Piecuch, Mehdi Moemeni, Aria Vahdani, Soham Maity, Babak Borhan, Marcos Dantus, Stephen H. Yuwono, Gary J. Blanchard, Briana A. Capistran
Publikováno v:
J Phys Chem B
Substituted fluorene structures have demonstrated unusual photochemical properties. Previous reports on the substituted fluorene Schiff base FR0-SB demonstrated super photobase behavior with a ΔpK(b) of ~14 upon photoexcitation. In an effort to unde
Publikováno v:
Journal of Polymer Science. 59:3181-3188
Autor:
Jessica S, Fortin, Kazuma, Shimanaka, A Prasanth, Saraswati, Mengyu, Liu, Kuang-Wei, Wang, Hsiao-Tien, Hagar, Soham, Maity, Susantha K, Ganegamage, Edmund, Ellsworth, Scott E, Counts, Babak, Borhan, Ulf, Dettmer, Min-Hao, Kuo
Publikováno v:
J Mol Struct
In contrast to Aβ plaques, the spatiotemporal distribution of neurofibrillary tangles of hyperphosphorylated tau (p-tau) predicts cognitive impairment in Alzheimer’s disease (AD), underscoring the key pathological role of p-tau and the utmost need
Autor:
Gary J. Blanchard, Soham Maity, Stephen H. Yuwono, Mehdi Moemeni, James E. Jackson, Marcos Dantus, Babak Borhan, Aria Vahdani, Piotr Piecuch, Briana A. Capistran
Publikováno v:
J Phys Chem B
Several fluorene derivatives exhibit excited-state reactivity and relaxation dynamics that remain to be understood fully. We report here the spectral relaxation dynamics of two fluorene derivatives to evaluate the role of structural modification in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2862cc4945374e595a25d12b097eb0e
https://europepmc.org/articles/PMC9273164/
https://europepmc.org/articles/PMC9273164/
Publikováno v:
Chemical record (New York, N.Y.). 21(10)
Nitroolefins are important synthetic intermediates in the field of organic synthesis as well as in medicinal chemistry. The high reactivity of nitroalkenes due to the polarized double bond which enables them to act as Michael acceptor in conjugate ad
Autor:
Jessica S. Fortin, Kazuma Shimanaka, A Prasanth Saraswati, Mengyu Liu, Kuang-Wei Wang, Hsiao-Tien Hagar, Soham Maity, Susantha K. Ganegamage, Edmund Ellsworth, Scott E. Counts, Babak Borhan, Ulf Dettmer, Min-Hao Kuo
Publikováno v:
Journal of Molecular Structure. 1267:133574
Publikováno v:
Polyhedron. 172:120-124
Aromatic nitro compounds are extensively used in synthetic chemistry. We disclose a new approach to obtain nitroarenes regioselectively starting from carboxylic acids under acid-free reaction conditions.
Autor:
Goutam Kumar Lahiri, Giuseppe Zanoni, Stefania Vergura, Alessio Baccalini, Debabrata Maiti, Farheen Fatima Khan, Siddhartha Maiti, Subhabrata Dutta, Pravas Dolui, Soham Maity
Publikováno v:
Organic Letters. 21:8842-8846
Unactivated olefins usually react poorly in conventional alkenylation reactions. Their introduction via C–H activation is limited to aromatic acids. Herein, we disclose a C–H functionalization prot...
Publikováno v:
Nature catalysis
α-Branched amines are present in hundreds of pharmaceutical agents and clinical candidates and are important targets for synthesis. Here we show the convergent synthesis of α-branched amines from three readily accessible starting materials: aromati