Diversity-oriented synthesis of analogues of the novel macrocyclic peptide FR-225497 through late stage functionalization

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• Dhatrak*, N. R.; Jagtap, A. B.; Shinde, T. N. doi:10.1002/0471264229.os099.23
• Albitz, K.; Csókás, D.; Dobi, Z.; Pápai, I.; Soós, T. Late‐Stage Formal Double C−H Oxidation of Prenylated Molecules to Alkylidene Oxetanes and Azetidines by Strain‐Enabled Cross‐Metathesis. Angewandte Chemie 2023, 135. doi:10.1002/ange.202216879
• Albitz, K.; Csókás, D.; Dobi, Z.; Pápai, I.; Soós, T. Late-Stage Formal Double C-H Oxidation of Prenylated Molecules to Alkylidene Oxetanes and Azetidines by Strain-Enabled Cross-Metathesis. Angewandte Chemie (International ed. in English) 2023, 62, e202216879. doi:10.1002/anie.202216879
• Auriostigue-Bautista, J. C.; Hernández-Vázquez, E.; González-Calderón, D.; Figueroa-Romero, J. L.; Castillo-Villanueva, A.; Torres-Arroyo, A.; Ponce-Macotela, M.; Rufino-González, Y.; Martínez-Gordillo, M.; Miranda, L. D.; Oria-Hernández, J.; Reyes-Vivas, H. Discovery of Benzopyrrolizidines as Promising Antigiardiasic Agents. Frontiers in cellular and infection microbiology 2022, 11, 828100. doi:10.3389/fcimb.2021.828100
• Chattopadhyay, S. K.; Ghosh, S.; Sarkar, S.; Bhadra, K. α,ß-Didehydrosuberoylanilide hydroxamic acid (DDSAHA) as precursor and possible analogue of the anticancer drug SAHA. Beilstein journal of organic chemistry 2019, 15, 2524–2533. doi:10.3762/bjoc.15.245
• Sarojini, V.; Cameron, A. J.; Varnava, K. G.; Denny, W. A.; Sanjayan, G. J. Cyclic Tetrapeptides from Nature and Design: A Review of Synthetic Methodologies, Structure, and Function. Chemical reviews 2019, 119, 10318–10359. doi:10.1021/acs.chemrev.8b00737
• Tyszka, A.; Pikus, G.; Dąbrowa, K.; Jurczak, J. Late-Stage Functionalization of ( R)-BINOL-Based Diazacoronands and Their Chiral Recognition of α-Phenylethylamine Hydrochlorides. The Journal of organic chemistry 2019, 84, 6502–6507. doi:10.1021/acs.joc.9b00630
• Chattopadhyay, S. K.; Ghosh, S.; Sil, S. Cross metathesis-mediated synthesis of hydroxamic acid derivatives. Beilstein journal of organic chemistry 2018, 14, 3070–3075. doi:10.3762/bjoc.14.285
• Jurczak, J.; Sobczuk, A.; Dabrowa, K.; Lindner, M.; Niedbała, P. An Indirect Synthetic Approach toward Conformationally Constrained 20-Membered Unclosed Cryptands via Late-Stage Installation of Intraannular Substituents. The Journal of organic chemistry 2018, 83, 13560–13567. doi:10.1021/acs.joc.8b02160
• Chattopadhyay, S. K.; Sil, S.; Mukherjee, J. P. Synthesis of 2-aminosuberic acid derivatives as components of some histone deacetylase inhibiting cyclic tetrapeptides. Beilstein journal of organic chemistry 2017, 13, 2153–2156. doi:10.3762/bjoc.13.214
• Herndon, J. W. The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2015 ☆. Coordination Chemistry Reviews 2016, 329, 53–162. doi:10.1016/j.ccr.2016.08.007
• Mukherjee, J. P.; Sil, S.; Chattopadhyay, S. K. Diversity‐Oriented Synthesis of Analogues of the Novel Macrocyclic Peptide FR‐225497 Through Late Stage Functionalization. ChemInform 2016, 47. doi:10.1002/chin.201605208

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