Great news!
If you didn't receive an email with the links, you can watch today's webinars on Youtube live by following this link:
https://t.co/mAbZExxbiN
See you on a few minutes! #LatinXChem2021#LatinXChem
Olá @LatinXChem Aquí meu trabalho de mestrado Caracterização in silico e in vitro da enzima SalC: Obtenção do intermediário oxidado usando sistema cell free. Pueden activar los subtitulos en español! (Aunque diga sub en portugues)#BIO115#LXChemBio https://t.co/ThS15eNwCP
Olá @LatinXChem e toda comunidade!! Este é o nosso trabalho entitulado "Síntese de novos selenetos-1,2,3-triazólícos com potencial atividade contra Trypanossoma cruzi"!! Estamos muito felizes em compartilhar nossa ciência com vocês ⚗️👩🔬🧪
#LatinXChem#LXChemOrg#OC042
olá @LatinXChem, este é meu trabalho "Obtenção da amida de Weinreb N-metoxi-N,2-dimetilbutanamida para síntese de tricetona assimétrica" #LatinXChem#LXChemOrg#OC131
Hi #LatinXChem👩🏽🔬🇧🇷 🇵🇪, I am glad to present to you our work "Biocatalysis and in silico study applied to asymmetric amine synthesis by transaminases". I am looking forward to your comments :)
@LatinXChem#LXChemBio#BIO068#LatinXChem2021 https://t.co/v9L5En58hF
#LatinXChem Webinars Serie is just around the corner.
Keep tuned for the information on how to register in these marvelous talks that we will have during the next week.
#LatinXChem#Webinars
Congratulations to all. #LatinXChem has become historical: the largest virtual chemical poster presentation event to showcase Latinx Chemistry. Thanks to all of you that make it possible.
@Alejand50635210@LatinXChem Hi Alejandra. Thank you.
Yes, i've made a few attempts to calculate the total conversion of the starting materials. Considering the yields of the synthesis of the substract plus the conversion of the biocatalytic part, i can say that the total conversion is close to 75% to 80%
@Daniel_G_Rivera@LatinXChem Thanks Daniel
I think that the fact that steric impediment is not very affected by the stereocenter configuration is the reason for the low influence on the stereoselectivity of the ring closing step.
@Daniel_G_Rivera@LatinXChem Hi Daniel. Thanks for reading my poster.
Well, the enzimes are responsable for the reductive
amination of the ketone. This reaction is enantioselective. However, the cyclization reaction can occur on both the re face and the si face. This causes moderate diasteroselectivity.