| Full text | |
| Author(s): |
Vasconcelos, Stanley N. S.
[1]
;
Shamim, Anwar
[2]
;
Ali, Bakhat
[1]
;
de Oliveira, Isadora M.
[3]
;
Stefani, Helio A.
[1]
Total Authors: 5
|
| Affiliation: | [1] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Farm, Sao Paulo, SP - Brazil
[2] Univ Sao Paulo, Inst Quim, Sao Paulo, SP - Brazil
[3] Univ Estadual Oeste Parana, Ctr Engn & Ciencias Exatas, Toledo, PR - Brazil
Total Affiliations: 3
|
| Document type: | Journal article |
| Source: | MOLECULAR DIVERSITY; v. 20, n. 2, p. 469-481, MAY 2016. |
| Web of Science Citations: | 2 |
| Abstract | |
1,2,3-Triazol tyrosines were synthesized from tyrosine alkynes that were in turn prepared via Sonogashira cross-coupling reaction. The tyrosine alkynes were subjected to click-chemistry reaction conditions leading to the corresponding 3-(1,2,3-triazolyl)-tyrosines in yields ranging from moderate to good. (AU) | |
| FAPESP's process: | 13/17960-7 - Functionalization of 3-iodo-(L)-Tyrosine via Suzuki-Miyaura Reaction Using Potassium Organotrifluoroborate salts |
| Grantee: | Stanley Nunes Siqueira Vasconcelos |
| Support Opportunities: | Scholarships in Brazil - Doctorate |
| FAPESP's process: | 12/00424-2 - Synthesis of small libraries using potassium Organotrifluoroborates in Suzuki-Miyaura reactions |
| Grantee: | Helio Alexandre Stefani |
| Support Opportunities: | Research Projects - Thematic Grants |