Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Pandiaraju, Subramanian"'
Autor:
Yekta, Shahla, Krasnova, Larissa B, Mariampillai, Brian, Picard, Christine J, Chen, Gang, Pandiaraju, Subramanian, Yudin, Andrei K
Publikováno v:
In Journal of Fluorine Chemistry 2004 125(4):517-525
Autor:
Brian J. Wilson, Methvin Isaac, Ayome Abibi, Michael Prakesch, Ratheesh Subramaniam, Ahmed Aman, Doug Kuntz, Rima Al-awar, Elijus Undzys, Justin Morin, Jeffrey Winston, Neil C. Pomroy, Craig Strathdee, Carly Griffin, Pandiaraju Subramanian, Herman Cheung, Gil G. Privé, Iain D. G. Watson, Taira Kiyota, Manuel Chan, Richard Marcellus, Anh Chau, Gennady Poda, Babu Joseph, David Uehling, Brigitte L. Thériault, Ahmed Mamai
Publikováno v:
Cancer Research. 79:7-7
The transcription factor B cell lymphoma 6 (BCL6) is required for the generation of an effective humoral immune response through the development and maintenance of germinal centers (GCs). The inhibition of the protein−protein interaction between BC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2715de60b777616a8c4dfd559d76036b
https://doi.org/10.1158/1538-7445.am2019-7
https://doi.org/10.1158/1538-7445.am2019-7
Publikováno v:
In Journal of Organometallic Chemistry 2000 603(1):98-104
Publikováno v:
Synthetic Communications. 39:2614-2624
3-Phenyl propylthiol esters were investigated as “activatable” solution phase linkers. These linkers can be activated with silver salts and upon treatment with amines can be converted to the corresponding amides. Under unactivated conditions, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::438512b81c953bfe7250f0b5d456e475
https://doi.org/10.1080/00397910802663352
https://doi.org/10.1080/00397910802663352
ChemInform Abstract: Rearrangement of 4-Amino-3-halo-pyridines by Nucleophilic Aromatic Substitution
Autor:
Doris Tang, Rima S. Al-awar, Pandiaraju Subramanian, M. Monzur Morshed, Iain D. G. Watson, Matthäus Getlik, Brian J. Wilson
Publikováno v:
ChemInform. 44
The reaction of 3-halo-4-aminopyridines with acyl chlorides and triethylamine is described. The pyridin-4-yl α-substituted acetamide products were obtained in moderate to high yields. The presented rearrangement reaction, in which the presumed N-acy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a925814f0fcf09c1b63b4ca709296d9
https://doi.org/10.1002/chin.201341164
https://doi.org/10.1002/chin.201341164
Autor:
Doris Tang, Matthäus Getlik, Rima S. Al-awar, M. Monzur Morshed, Pandiaraju Subramanian, Iain D. G. Watson, Brian J. Wilson
Publikováno v:
The Journal of organic chemistry. 78(11)
The reaction of 3-halo-4-aminopyridines with acyl chlorides and triethylamine is described. The pyridin-4-yl α-substituted acetamide products were obtained in moderate to high yields. The presented rearrangement reaction, in which the presumed N-acy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf6ff095e4f219cf3602b8819df2623a
https://pubmed.ncbi.nlm.nih.gov/23700973
https://pubmed.ncbi.nlm.nih.gov/23700973
Publikováno v:
ChemInform. 40
3-Phenyl propylthiol esters were investigated as “activatable” solution phase linkers. These linkers can be activated with silver salts and upon treatment with amines can be converted to the corresponding amides. Under unactivated conditions, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40f41b84fdf0e3fab4abf565cb0970e5
https://doi.org/10.1002/chin.200951058
https://doi.org/10.1002/chin.200951058
Publikováno v:
Israel Journal of Chemistry; 2001, Vol. 41 Issue 4, p309-312, 4p
Autor:
Basavaiah, Deevi, Krishnamacharyulu, Marimganti, Hyma, Rachakonda Suguna, Pandiaraju, Subramanian
Publikováno v:
Tetrahedron Letters; January 1997, Vol. 38 Issue: 12 p2141-2144, 4p
Publikováno v:
ChemInform; Oct2000, Vol. 31 Issue 43, pno-no, 1p