Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bruno B. Ravanello"'
Publikováno v:
Pharmaceutics, Vol 11, Iss 2, p 59 (2019)
Herein, a new Ugi multicomponent reaction strategy is described to enhance activity and solubility of the chemotherapeutic drug chlorambucil through its conjugation to poly(amidoamine) (PAMAM-NH2) dendrimers with the simultaneous introduction of lipi
Externí odkaz:
https://doaj.org/article/6b58bc571e664c57b0a1986ce32c2cda
Autor:
Roberto Christ Vianna Santos, Luciano Dornelles, Guerino Bandeira Junior, Bruno B. Ravanello, Rodrigo de Almeida Vaucher, Oscar E. D. Rodrigues, Bernardo Baldisserotto, Rafael S. da Silva, Victor dos Santos Barboza, Fernanda H. da Rosa, Letiére Cabreira Soares
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 151:377-383
Herein, we present a new variation for an eco-friendly methodology for the synthesis of chalcogenoester in good-to-excellent yields in a short time, with an easy work-up/purification step, and in a greenest methodology, affording the minimum generati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70ea1c8fb1ce0881bb1aa8791f2fba13
https://doi.org/10.1007/s00706-020-02565-x
https://doi.org/10.1007/s00706-020-02565-x
Autor:
Keiti Oliveira Alessio, Ionara I. Dalcol, Fabio A. Duarte, Nalin Seixas, Ademir F. Morel, Vanessa Bender, Bruno B. Ravanello
Publikováno v:
Current Organic Chemistry. 23:2131-2140
Triterpenes and phytosterols are classes of natural compounds widespread in plants possessing a great number of pharmacological activities. In our continued search for new compounds from natural sources with pharmacological potential, we prepared a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe7fc34e0b946f4a49632a2e8df89989
https://doi.org/10.2174/1385272823666191014154939
https://doi.org/10.2174/1385272823666191014154939
Autor:
Nalin, Seixas, Bruno B, Ravanello, Ibrahim, Morgan, Goran N, Kaluđerović, Ludger A, Wessjohann
Publikováno v:
Pharmaceutics
Herein, a new Ugi multicomponent reaction strategy is described to enhance activity and solubility of the chemotherapeutic drug chlorambucil through its conjugation to poly(amidoamine) (PAMAM-NH2) dendrimers with the simultaneous introduction of lipi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::09eb766cbf691a4fdcb33e21c9daf86a
https://pubmed.ncbi.nlm.nih.gov/30717083
https://pubmed.ncbi.nlm.nih.gov/30717083
Autor:
Rafael S. da Silva, Bernhard Westermann, Andrej Frolov, Bruno B. Ravanello, Daniel G. Rivera, Nalin Seixas, Marcos A. Villetti, Oscar E. D. Rodrigues
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 24(39)
Aiming at providing an efficient and versatile method for the diversity-oriented decoration and ligation of fullerenes, we report the first C60 derivatization strategy based on isocyanide-multicomponent reactions (I-MCRs). The approach comprises the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b514ddc96fc01ad506ca819c07df410
https://pubmed.ncbi.nlm.nih.gov/29882608
https://pubmed.ncbi.nlm.nih.gov/29882608
Autor:
Roberto Christ Vianna Santos, Rodrigo de Almeida Vaucher, Letiére C. Soares, Oscar E. D. Rodrigues, Camilla Filippi dos Santos Alves, Luciano Dornelles, Senthil Narayanaperumal, Taiane Schneider, Bruno B. Ravanello, Josimar Vargas, Kashif Gul
Publikováno v:
Tetrahedron. 68:10444-10448
Efficient ring opening reaction between aziridines and diphenyl dichalogenides using HCl, Zn° in ionic liquid is disclosed, affording chiral β-chalcogen amines derivatives in good yields under mild reaction condition. The ionic liquid was further r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d889bdd68f7fe11a0ac04eae32c3364
https://doi.org/10.1016/j.tet.2012.09.049
https://doi.org/10.1016/j.tet.2012.09.049