Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Sivaji Gundala"'
Autor:
Eric Block, Benjamin Bechand, Sivaji Gundala, Abith Vattekkatte, Kai Wang, Shaymaa S. Mousa, Kavitha Godugu, Murat Yalcin, Shaker A. Mousa
Publikováno v:
Molecules, Vol 28, Iss 3, p 1025 (2023)
In the original publication [...]
Externí odkaz:
https://doaj.org/article/390bbafffbba4cf6a16311984972c95a
Autor:
Aashutosh Vihani, Xiaoyang Serene Hu, Sivaji Gundala, Sachiko Koyama, Eric Block, Hiroaki Matsunami
Publikováno v:
eLife, Vol 9 (2020)
Understanding how genes and experience work in concert to generate phenotypic variability will provide a better understanding of individuality. Here, we considered this in the main olfactory epithelium, a chemosensory structure with over a thousand d
Externí odkaz:
https://doaj.org/article/72239086c38d47c4ae9ceb71183df50a
Autor:
Eric Block, Benjamin Bechand, Sivaji Gundala, Abith Vattekkatte, Kai Wang, Shaymaa S. Mousa, Kavitha Godugu, Murat Yalcin, Shaker A. Mousa
Publikováno v:
Molecules, Vol 22, Iss 12, p 2081 (2017)
We describe the synthesis, reactivity, and antithrombotic and anti-angiogenesis activity of difluoroallicin (S-(2-fluoroallyl) 2-fluoroprop-2-ene-1-sulfinothioate) and S-2-fluoro-2-propenyl-l-cysteine, both easily prepared from commercially available
Externí odkaz:
https://doaj.org/article/5f03de18eead4a57aa50d40e21aea8f3
Autor:
Hiroaki Matsunami, Aashutosh Vihani, Sachiko Koyama, Xiaoyang Serene Hu, Eric Block, Sivaji Gundala
Publikováno v:
eLife, Vol 9 (2020)
eLife
eLife
Understanding how genes and experiences work in concert to generate phenotypic variability will provide a better understanding of individuality. Here, we considered this in the context of the main olfactory epithelium, a chemosensory structure with o
Autor:
M. Jake Pushie, Rama Yaghi, Jun Liu, Stephene N. Lodge, Graham N. George, Sharon Rozovsky, Sonia Flores-Penalba, Bradley J. Landgraf, Sivaji Gundala, Huawei Zeng, Squire J. Booker, Abith Vattekkatte, Eric Block
Publikováno v:
ChemBioChem. 17:1738-1751
Trifluoroselenomethionine (TFSeM), a new unnatural amino acid, was synthesized in seven steps from N-(tert-butoxycarbonyl)-l-aspartic acid tert-butyl ester. TFSeM shows enhanced methioninase-induced cytotoxicity, relative to selenomethionine (SeM), t
Publikováno v:
Org. Biomol. Chem.. 14:3040-3046
It has been shown for the first time that enolisable anhydrides can participate in highly efficient and diastereo/enantioselective additions to activated ketones. In these reactions the anhydride component formally acts (initially) as the nucleophili
Autor:
Michael J. Corr, Hanyi Zhuang, Hiroaki Matsunami, Lucky Ahmed, Eric Block, Qingzhi Zhang, M. Buehl, Mingan Wang, Nicholas S. Ten, Yuetian Zhang, Sivakumar Sekharan, Rodrigo A. Cormanich, Yi Pan, David O'Hagan, Mingyan Yang, Victor S. Batista, Mehmet Ozbil, Ruina Zhang, Sivaji Gundala
We acknowledge support from NSF (CHE-1265679) and NIH (5R01DC014423 subaward) (EB), NIH (5R01 DC014423) (HM), the European Reasearch Council (ERC) and the Engineering Science Research Council (EPSRC) (DO'H), FAPESP and CNPq (RAC), the Chinese Scholar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ccced171bc0c5dae04dd3a315c6fa77
https://hdl.handle.net/10023/16171
https://hdl.handle.net/10023/16171
Autor:
Abith Vattekkatte, Eric Block, Benjamin Bechand, Murat Yalcin, Shaymaa S Mousa, Kavitha Godugu, Kai Wang, Shaker A. Mousa, Sivaji Gundala
Publikováno v:
Molecules; Volume 22; Issue 12; Pages: 2081
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 22, Iss 12, p 2081 (2017)
Molecules : A Journal of Synthetic Chemistry and Natural Product Chemistry
Molecules, Vol 22, Iss 12, p 2081 (2017)
We describe the synthesis, reactivity, and antithrombotic and anti-angiogenesis activity of difluoroallicin (S-(2-fluoroallyl) 2-fluoroprop-2-ene-1-sulfinothioate) and S-2-fluoro-2-propenyl-l-cysteine, both easily prepared from commercially available
Publikováno v:
Synlett. 24:1225-1228
The first organocatalytic aerobic oxidative cleavage of cyclic 1,2-diketones is reported. The reaction occurs in either aqueous or alcoholic media and is promoted by a simple N-heterocyclic carbene catalyst derived from a 1,2,4-triazolium ion. No str