Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Irshad Maajid Taily"'
Autor:
Alexander J. Lander, Laura Domínguez Mercado, Xuefei Li, Irshad Maajid Taily, Brandon L. Findlay, Yi Jin, Louis Y. P. Luk
Publikováno v:
Communications Chemistry, Vol 6, Iss 1, Pp 1-7 (2023)
Abstract Tryptophan is frequently found on the surface of membrane-associated proteins that interact with the lipid membrane. However, because of their multifaceted interactions, it is difficult to pinpoint the structure-activity relationship of each
Externí odkaz:
https://doaj.org/article/6d0f8cfe77604de78e87727469801653
Autor:
Nirmal Kumar, Irshad Maajid Taily, Charandeep Singh, Sahil Kumar, Raju S Rajmani, Debajyoti Chakraborty, Anshul Sharma, Priyanka Singh, Krishan Gopal Thakur, Raghavan Varadarajan, Rajesh P Ringe, Prabal Banerjee, Indranil Banerjee
Publikováno v:
PLoS Pathogens, Vol 19, Iss 5, p e1011358 (2023)
Rapid evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and influenza A virus (IAV) poses enormous challenge in the development of broad-spectrum antivirals that are effective against the existing and emerging viral strains. V
Externí odkaz:
https://doaj.org/article/10c226cafb564cada610602350982a35
Publikováno v:
Organic Letters. 24:2310-2314
The synthesis of paracetamol still relies on multistep protocols involving the utilization of a stoichiometric amount of oxidizing/reducing or other corrosive agents. Herein we report a regioselective electrochemical Ritter-type reaction at the C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e000b303d24044d914786ef49d106ea
https://doi.org/10.1021/acs.orglett.2c00439
https://doi.org/10.1021/acs.orglett.2c00439
Publikováno v:
Chemical Communications. 58:5459-5462
An external oxidant free electrochemical strategy is designed towards the β-scission of strained C–C bonds in cyclopropylamine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40da0d2b09fd6185117547d0e93f1b0a
https://doi.org/10.1039/d2cc00761d
https://doi.org/10.1039/d2cc00761d
Publikováno v:
Chemical communications (Cambridge, England).
The site-selective C-H functionalization of arenes is of indisputable importance in organic chemistry. Herein, we have demonstrated an electrochemical regioselective oxidative cross-coupling towards the direct C(sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6aa22caead2d757de57357ee3fa1a45f
https://pubmed.ncbi.nlm.nih.gov/36507914
https://pubmed.ncbi.nlm.nih.gov/36507914
Publikováno v:
European Journal of Organic Chemistry. 2021:5053-5057
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f82be38b4358401d11ab161dd792deb
https://doi.org/10.1002/ejoc.202101022
https://doi.org/10.1002/ejoc.202101022
Publikováno v:
Chemical Communications. 57:2464-2478
Rearrangement reactions constitute a critical facet of synthetic organic chemistry and demonstrate an attractive way to take advantage of existing structures to access various important molecular frameworks. Electroorganic chemistry has emerged as an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b0a5dabbdfdd4f65492bda76b9aebc5
https://doi.org/10.1039/d1cc00116g
https://doi.org/10.1039/d1cc00116g
Publikováno v:
Chemical Communications. 57:631-634
Isocyanates are the key intermediates for several organic transformations towards the synthesis of diverse pharmaceutical targets. Herein, we report the development of an oxidant-free protocol for electrochemical in situ generation of isocyanates. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2bfa270326e3f19c47fe717dafb25980
https://doi.org/10.1039/d0cc07125k
https://doi.org/10.1039/d0cc07125k
Publikováno v:
The Journal of organic chemistry. 87(5)
Herein, we report a highly facile and unprecedented activation of 3-amido oxetanes to synthesize 2-oxazoline amide ethers using a transient electrophilic aza-oxyallyl cation as an activating as well as an alkylating agent under mild reaction conditio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e68266023774d6ddc9bf393a78e68c20
https://pubmed.ncbi.nlm.nih.gov/35129349
https://pubmed.ncbi.nlm.nih.gov/35129349
Publikováno v:
European Journal of Organic Chemistry. 2019:7804-7813
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecb85ce650d2ed3eff7b64793a1601df
https://doi.org/10.1002/ejoc.201901400
https://doi.org/10.1002/ejoc.201901400