Multicyclic Peptides via Templated Tandem CLIPS/CuAAC Cyclizations

Autor: Richelle, G., Schmidt, M., Hiemstra, H., Nuijens, T., van Maarseveen, J., Timmerman, P.

Publikováno v: Journal of Peptide Science, 24(S2):P225. John Wiley and Sons Ltd

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::00647627ed0afabf4a26e095a0af91c3
https://dare.uva.nl/personal/pure/en/publications/multicyclic-peptides-via-templated-tandem-clipscuaac-cyclizations(991b93f5-f190-416b-8973-19f901d6a18f).html

Hetero-Diels–Alder and CuAAC Click Reactions for Fluorine-18 Labeling of Peptides: Automation and Comparative Study of the Two Methods.

Autor: Maujean, Timothé¹ (AUTHOR), Ramanoudjame, Sridévi M.¹ (AUTHOR), Riché, Stéphanie¹ (AUTHOR), Le Guen, Clothilde^1,2 (AUTHOR), Boisson, Frédéric³ (AUTHOR), Muller, Sylviane⁴ (AUTHOR), Bonnet, Dominique¹ (AUTHOR), Gulea, Mihaela¹ (AUTHOR), Marchand, Patrice³ (AUTHOR) patrice.marchand@iphc.cnrs.fr

Publikováno v: Molecules. Jul2024, Vol. 29 Issue 13, p1-14. 14p. 2 Charts.

Enantioselective propargylic amination and related tandem sequences to α-tertiary ethynylamines and azacycles.

Autor: Zhang Z; State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China., Sun Y; State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China., Gong Y; State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China., Tang DL; State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China., Luo H; State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China., Zhao ZP; State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China., Zhou F; State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China. fzhou@chem.ecnu.edu.cn., Wang X; College of Chemistry, Sichuan University, Chengdu, China. wangxin@scu.edu.cn., Zhou J; State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, China. jzhou@chem.ecnu.edu.cn.; College of Chemistry and Molecular Sciences, Henan University, Kaifeng, China. jzhou@chem.ecnu.edu.cn.; State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Shanghai, P. R. China. jzhou@chem.ecnu.edu.cn.

Publikováno v: Nature chemistry [Nat Chem] 2024 Apr; Vol. 16 (4), pp. 521-532. Date of Electronic Publication: 2024 Mar 19.

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Switchable Synthesis of 7‐ and 14‐Membered Cyclic Peptides Containing N‐Methyl‐ and β‐Amino Acids Utilizing Microflow Technology.

Autor: Fuse, Shinichiro¹ (AUTHOR) fuse@ps.nagoya-u.ac.jp, Okabe, Ren¹ (AUTHOR)

Publikováno v: European Journal of Organic Chemistry. 9/14/2023, Vol. 26 Issue 35, p1-5. 5p.