Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Evangelina Repetto"'
Autor:
María Emilia Cano, Walter Emiliano Jara, Alejandro J. Cagnoni, Emmanuel Brizzio, Miriam C. Strumia, Evangelina Repetto, María Laura Uhrig
Publikováno v:
New Journal of Chemistry. 46:17682-17695
S-Glycosylated dendrons having a thioacetate group in their focal points led to multivalent glycoclusters by spontaneous O2-oxidation of sulfides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f247417cdd7f3e2f2afed7a82f70a3b
https://doi.org/10.1039/d2nj03071c
https://doi.org/10.1039/d2nj03071c
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa4a602817e26217a624109c3bc71146
https://doi.org/10.1002/ejoc.202200589
https://doi.org/10.1002/ejoc.202200589
Autor:
Aashruti Agrawal, Rascón-Chu Agustín, Hanan B. Ahmed, Bhavna Alke, Sánchez-Villegas J. Alfonso, Sukumaran Anil, Balaprasad Ankamwar, Geeta Arya, Rajib Bandopadhyay, Raju Biswas, Mengna Cao, Soma Chakraborty, Norma B. D'Accorso, Pandurang A. Dalavi, Anurag Dutta, Hossam E. Emam, Shahira M. Ezzat, Ohlmaier-Delgadillo Federico, Gomez-Rodriguez Gabriel H., Dipak D. Gadade, Nancy Lis Garcia, Qing Gu, Félix-Arias K. Guadalupe, Nidhi Gupta, Surabhi Gupta, Yusuf Haggag, Urmi Halder, Xiuting Hu, Harsha Jain, Supriya Jain, M.V. Jithin, Renjith P. Johnson, Ashutosh Kabiraj, Deepak A. Kulkarni, Mikhail I. Kusayin, Moitri Let, Lara-Espinoza Claudia Lizeth, Jitender Madan, Krishnendu Majhi, Verónica E. Manzano, Shirui Mao, Ming Miao, D.B. Mondal, Sesha Subramanian Murugan, Fangfang Ni, Surendra Nimesh, Purva Pingle, Ashwini Prabhu, Namitha K. Preman, Pradipta Purkayastha, R. Raguavaran, Carlos Rodriguez Ramirez, Vinitha Rani, Anton B. Rasin, Pavan B. Rathi, Evangelina Repetto, Mohamed A. Salem, Jaiprakash N. Sangshetti, Sandesh G. Sanjeeva, Jayanta K. Sarmah, Sanjib Sarmah, D.K. Sharma, Lokesh Sharma, Saurabh Shrivastava, Yujiao Sun, Usman T. Syed, Chandrakant Tagad, Syed N. Taqui, Shareefraza J. Ukkund, Roland Ulber, Rosa V. Usoltseva, Jayachandran Venkatesan, Hujun Xie, Awesh K. Yadav, Narayani Yadav, Ahmed Zayed, Gomeztagle-Romero M. Zuleth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e76d93ca638052ec742a2a338b5b1673
https://doi.org/10.1016/b978-0-12-822351-2.00099-1
https://doi.org/10.1016/b978-0-12-822351-2.00099-1
Autor:
Ahmed S. Abo Dena, Caleb Acquah, Tanvir Ahmed, Azilah Ajit, Yahya S. Al-Awthan, Tânia Albuquerque, Sukumaran Anil, Nuvia Marina Apolonio–Hernandez, Leonard Ionut Atanase, Omar Bahattab, Anindita Behera, Muhammad Bilal, Branko Bugarski, A.C. Campa-Mada, Ireri Alejandra Carbajal-Valenzuela, E. Carvajal-Millan, Long Chen, Wai Teng Cheng, Custodiana A. Colmenarez Lobo, Diana Costa, Eduardo Costa, Pandurang Appana Dalavi, Michael K. Danquah, Y. De Anda-Flores, Harshal Deshmukh, Amal Kumar Dhara, Ibrahim M. El-Sherbiny, Rúben Faria, Ana Angelica Feregrino-Pérez, M.D. Figueroa-Pizano, D.A.S. Gamage, Beatriz González-Arias, Natanamurugaraj Govindan, Ramón Gerardo Guevara-González, Diana Vanesa Gutierrez-Chavez, Md Saquib Hasnain, Shafiul Hossain, Muhammad Imran, Hafiz M.N. Iqbal, Jaison Jeevanandam, Alejandra Jimenez-Hernandez, Zhengyu Jin, Sumaya F. Kabir, Krishnan Kanny, Jaya Lakkakula, J. Lizardi-Mendoza, Manuela Machado, T. Madhujith, Gaanty Pragas Maniam, Verónica E. Manzano, A.L. Martínez-López, K.G. Martínez-Robinson, David Julian McClements, Ming Miao, Milan Milivojevic, Md. Minhajul Islam, Aurelie Sarah Mok Tsze Chung, Mohammad S. Mubarak, Naveed Muhammad, Hira Munir, Sesha Subramanian Murugan, Amit Kumar Nayak, Ana R. Neves, Ahmed Olatunde, Ivana Pajic-Lijakovic, Dilipkumar Pal, Aristeidis Papagiannopoulos, Manuela Pintado, Marcel Popa, Sarmad Ahmad Qamar, Telma Quintela, Stefania Racovita, Hamza Rafeeq, Mohd Hasbi Ab. Rahim, Ashiqur Rahman, Mohammed Mizanur Rahman, Khushboo Raj, Ajay Vasudeo Rane, A. Rascón-Chu, Abdur Rauf, Evangelina Repetto, Enrique Rico-García, Supriyo Saha, Md. Sazedul Islam, Md. Shahruzzaman, Sara Silva, Ângela Sousa, Ahmad Ziad Sulaiman, Sabrina Sultana, Joash Ban Lee Tan, J. Tanori-Cordova, Yong Kiat Teo, Himja Tiwari, Irineo torres-Pacheco, Tabussam Tufail, Silvia Vasiliu, Jayachandran Venkatesan, Eleni Vlassi, Nilesh Shirish Wagh, N.E. Wedamulla, Deepti Yadav, Zhongyu Yang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ff538ce0aba38e4fbd153c7c04389c3
https://doi.org/10.1016/b978-0-323-85759-8.00031-2
https://doi.org/10.1016/b978-0-323-85759-8.00031-2
Publikováno v:
ChemistrySelect. 2:4774-4778
The major endo cycloadducts with a basic structure of methyl 1-aryl-3-(benzyl or methyl)-6-menthyloxy-7-oxooctahydropyrano[4,3-c]pyrrole-3-carboxylate were subjected to simple chemical transformations (mostly reduction and hydrolysis reactions) to af
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::537b94b557ab8f297d7342a26a825c7e
https://doi.org/10.1002/slct.201701068
https://doi.org/10.1002/slct.201701068
Publikováno v:
Carbohydrate Research. 483:107751
A 6-azido-2-tosylenolate, obtained from D-glucono-1,5-lactone in six steps, underwent an intramolecular cycloaddition–elimination pathway under mild conditions, yielding a chiral, substituted 5,6-dihydro-4H-pyrrolo[1,2-c]-1,2,3-triazole. The condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b36faff2d0abc7c23b42d0ce752fb56d
https://doi.org/10.1016/j.carres.2019.107751
https://doi.org/10.1016/j.carres.2019.107751
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Enantiomeric 2,3,4-tris(hydroxyalkyl)-5-phenylpyrrolidines have been synthesized from the major cycloadducts obtained by the 1,3-dipolar cycloaddition of sugar enones with azomethine ylides derived from natural amino acids. Reduction of the ketone ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48abc16e2d53a2806e4d2219ba886065
https://pubmed.ncbi.nlm.nih.gov/27116655
https://pubmed.ncbi.nlm.nih.gov/27116655
Publikováno v:
The Journal of Organic Chemistry. 77:253-265
Satisfactory procedures are described for the synthesis of 5,6- and 3,4-thiirane derivatives from the respective hexofuranose or hexopyranose epoxide precursors. The controlled ring-opening reaction of thiiranes by 1-thioaldoses was successfully acco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3c25a5e4a806cc8ab64b265548889da
https://doi.org/10.1021/jo2018685
https://doi.org/10.1021/jo2018685