Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Pandi Muthupandi"'
Autor:
Jenna L. Clements, Franziska Pohl, Pandi Muthupandi, Stephen C. Rogers, Jack Mao, Allan Doctor, Vladimir B. Birman, Jason M. Held
Publikováno v:
Redox Biology, Vol 37, Iss , Pp 101707- (2020)
S-nitrosation of cysteine thiols (SNOs), commonly referred to as S-nitrosylation, is a cysteine oxoform that plays an important role in cellular signaling and impacts protein function and stability. Direct labeling of SNOs in cells with the flexibili
Externí odkaz:
https://doaj.org/article/eb6f5219e21f48d8bd7d8ab581bdcec2
Publikováno v:
In Applied Catalysis A, General 28 October 2012 441-442:119-123
Publikováno v:
The Journal of Organic Chemistry. 82:1936-1942
An efficient domino reaction has been developed for the synthesis of thiochromenes through Cu-catalyzed in situ incorporation of sulfur. This domino method avoids the use of less accessible and unpleasant arenethiols as starting materials, instead ut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20a375148579945ae46d46bae67b8f91
https://doi.org/10.1021/acs.joc.6b02740
https://doi.org/10.1021/acs.joc.6b02740
Publikováno v:
Journal of the American Chemical Society. 142(1)
We introduce phenazine-1,6-dicarboxamides as redox-responsive molecular switches. The reduction of their phenazine core transforms them from hydrogen-bond acceptors into hydrogen-bond donors and thus forces the secondary amide substituents to turn ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dba3ddf150d81960ed06caf84c4c9e8
https://pubmed.ncbi.nlm.nih.gov/31873004
https://pubmed.ncbi.nlm.nih.gov/31873004
Autor:
Franziska Pohl, Jenna L. Clements, Vladimir B. Birman, Stephen C. Rogers, Allan Doctor, Pandi Muthupandi, Jason M. Held, Jack Mao
Publikováno v:
Redox Biology, Vol 37, Iss, Pp 101707-(2020)
Redox Biology
Redox Biology
S-nitrosation of cysteine thiols (SNOs), commonly referred to as S-nitrosylation, is a cysteine oxoform that plays an important role in cellular signaling and impacts protein function and stability. Direct labeling of SNOs in cells with the flexibili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f63311763b7afcb64bac75c2603aa829
https://doi.org/10.1016/j.redox.2020.101707
https://doi.org/10.1016/j.redox.2020.101707
Publikováno v:
Organic Letters. 17:5448-5451
A domino process that converges the migratory insertion of carbene with a Heck reaction has been established as a versatile tool for the synthesis of 2-arylidene-3-aryl-1-indanones from very stable and easily accessible N-tosylhydrazones and 2'-iodoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efe709a5068338ec77c6371d78e8b480
https://doi.org/10.1021/acs.orglett.5b02803
https://doi.org/10.1021/acs.orglett.5b02803
Publikováno v:
Organic letters. 19(24)
A tandem rearrangement of α,β-unsaturated thioesters into tricyclic ene-lactones fails with conventional amidine-based catalysts, but becomes possible when their electron-rich analogs are employed. A highly diastereo- and enantioselective version o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::954d000c1433040639af2958c775115e
https://pubmed.ncbi.nlm.nih.gov/29200308
https://pubmed.ncbi.nlm.nih.gov/29200308
Publikováno v:
ChemInform. 47
An efficient domino process for the synthesis of thioflavanones has been described using a copper catalyst without addition of any external ligand. A variety of thioflavanones have been synthesized from easily accessible 2′-iodochalcones or 2′-br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01646d250be861a7a6a91a242ab8e8f8
https://doi.org/10.1002/chin.201618145
https://doi.org/10.1002/chin.201618145
Publikováno v:
ChemInform. 47
Tosylhydrazones from arylaldehydes and 2-iodochalcones react under Pd catalysis to give the title compounds in high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::731ca5a1f54bb35d6a9002035e786d6d
https://doi.org/10.1002/chin.201612117
https://doi.org/10.1002/chin.201612117
Publikováno v:
Organic letters. 17(24)
An efficient domino process for the synthesis of thioflavanones has been described using a copper catalyst without addition of any external ligand. A variety of thioflavanones have been synthesized from easily accessible 2′-iodochalcones or 2′-br
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f61d2bd88786a6127432207789951ffa
https://pubmed.ncbi.nlm.nih.gov/26642368
https://pubmed.ncbi.nlm.nih.gov/26642368