Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Manuel A. Rentería-Gómez"'
Autor:
Alejandro Corona-Díaz, Diana G. García García, Shirikant G. Pharande, Manuel A. Rentería-Gómez, Rocío Gámez-Montaño
Publikováno v:
Chemistry Proceedings, Vol 12, Iss 1, p 79 (2022)
2,5-DKPs are heterocyclic peptidomimetics, present in nature with high structural diversity, popular in the design of new bioactive molecules with potential application in medicinal chemistry, exhibiting anticancer and antimicrobial properties, among
Externí odkaz:
https://doaj.org/article/9b0ff43ee9874758b2b2334af373d746
Publikováno v:
Chemistry Proceedings, Vol 8, Iss 1, p 42 (2021)
A series of ten 1,5-disubstituted-1H-tetrazoles (1,5-DS-T) were synthesized via Ugi-azide isocyanide-based multicomponent reactions (IMCR) in low to good yields (30–85%), using propargyl amine or 2-azidobenzaldehyde as a component, and using ultras
Externí odkaz:
https://doaj.org/article/3146f71cd77a4b4d9d29cf8fb1260965
Autor:
Manuel A. Rentería-Gómez, Alejandro Islas-Jácome, Shrikant G. Pharande, David A. Vosburg, Rocío Gámez-Montaño
Publikováno v:
Frontiers in Chemistry, Vol 7 (2019)
6-Triazolylmethyl-pyrrolo[3,4-b]pyridin-5-one tris-heterocycles were synthesized in 43–57% overall yields. The two-stage synthesis involved a cascade process (Ugi-3CR/aza Diels-Alder/N-acylation/aromatization) followed by a copper-assisted alkyne-a
Externí odkaz:
https://doaj.org/article/6deb07ef356745bcad7c596f3967523d
Publikováno v:
Molecules, Vol 25, Iss 22, p 5246 (2020)
A novel strategy via the triple process (multicomponent reactions (MCR)-domino)/tandem was developed for the synthesis of restricted and constrained bis-1,2,3-triazole-linked pyrrolo[3,4-b]pyridine peptidomimetics dimers in overall yields of 20–55%
Externí odkaz:
https://doaj.org/article/532ebde1a4ff402f8f728726696933d1
Autor:
Manuel A. Rentería-Gómez, Shrikant G. Pharande, Alejandro Islas-Jácome, Eduardo González-Zamora, Rocío Gámez-Montaño
Publikováno v:
Proceedings, Vol 9, Iss 1, p 5 (2019)
An efficient Microwave (MW)-assisted synthesis of eight new 6-nitrilmethyl-pyrrolo[3,4-b]pyridin-5-ones via a domino process: aza Diels–Alder/N-acylation/aromatization (dehydration–decarboxylation) from their corresponding 2-aminonitrile-oxazoles
Externí odkaz:
https://doaj.org/article/7f719f56b5ad4460bd8208290b93b08c
Autor:
Michelle Lee, Nathan J. Vosburg, Emily A. Shimizu, Manuel A. Rentería-Gómez, Rocío Gámez-Montaño, David A. Vosburg
Publikováno v:
Journal of Chemical Education. 99:2399-2402
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cf31bd024ec9d14b32eaa99a9d407bd
https://doi.org/10.1021/acs.jchemed.2c00143
https://doi.org/10.1021/acs.jchemed.2c00143
Publikováno v:
New Journal of Chemistry. 46:9298-9303
A facile, rapid, sustainable one-pot Diversity Oriented Synthesis of peptidomimetics via mechanochemical IMCR-based domino strategies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1d1f4783475d88b7d6e30c6d3874108
https://doi.org/10.1039/d1nj05994g
https://doi.org/10.1039/d1nj05994g
Autor:
Sandra C. Ramírez-López, Manuel A. Rentería-Gómez, Cesar R. Solorio Alvarado, Rocío Gámez-Montaño
Publikováno v:
The 24th International Electronic Conference on Synthetic Organic Chemistry.
A series of three 2,5-Diketopiperazine (DKPs) were synthesized via one-pot process through the post- isocyanide-based multicomponent reactions (IMCR)-transformation strategy. This strategy emphasizes the role of orthogonal bifunctional reagents in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1c244e985eacc9caf50a3f2e60d76b9
https://doi.org/10.3390/ecsoc-24-08396
https://doi.org/10.3390/ecsoc-24-08396
Publikováno v:
The 24th International Electronic Conference on Synthetic Organic Chemistry.
A series of six novel amide-xanthate products containing several fluorine atoms were prepared in moderate to good yields (40–92%) via an isocyanide-based multicomponent reaction (IMCR) of 5-CR by Ugi-4CR followed by an SN2 sequence in a one-pot man
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34a650865e2cca5ddd1e732cb9561868
https://doi.org/10.3390/ecsoc-24-08421
https://doi.org/10.3390/ecsoc-24-08421
Publikováno v:
Molecules
Volume 25
Issue 22
Molecules, Vol 25, Iss 5246, p 5246 (2020)
Volume 25
Issue 22
Molecules, Vol 25, Iss 5246, p 5246 (2020)
A novel strategy via the triple process (multicomponent reactions (MCR)-domino)/tandem was developed for the synthesis of restricted and constrained bis-1,2,3-triazole-linked pyrrolo[3,4-b]pyridine peptidomimetics dimers in overall yields of 20&ndash
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ec3f9f471ed45c2d46b708c864a8a7c