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- Highly efficient one-pot assembly of peptides by double chemoselective coupling. Ivo E. Sampaio-Dias, Carlos A. D. Sousa, Sara C. Silva-Reis, Sara Ribeiro, Xerardo García-Mera, José E. Rodríguez-Borges
, Org. Biomol. Chem.
, 2017
, 15
, 7533
- Solvent free, catalytic and diastereoselective preparation of aryl and alkyl thioglycosides as key components for oligosaccharide synthesis. Daniel L. Jensen, Helle H. Trinderup, Frederik Skovbo, Henrik H. Jensen
, Org. Biomol. Chem.
, 2022
, 20
, 4915
- Synthesis of substituted exo-glucals via a modified Julia olefination and identification as selective β-glucosidase inhibitors. Samuel Habib, Florent Larnaud, Emmanuel Pfund, Teresa Mena Barragán, Thierry Lequeux, Carmen Ortiz Mellet, Peter G. Goekjian, David Gueyrard
, Org. Biomol. Chem.
, 2014
, 12
, 690
- An enzymatic approach to bifunctional chelating agents. Paolo Minazzi, Luciano Lattuada, Ivan G. Menegotto, Giovanni B. Giovenzana
, Org. Biomol. Chem.
, 2014
, 12
, 6915
- Metal carbonyl mediated rearrangement of 5-(2-oxoalkyl)-1,2,4-oxadiazoles: synthesis of fully substituted pyrimidines. Ekaterina E. Galenko, Timur O. Zanakhov, Mikhail S. Novikov, Alexander F. Khlebnikov
, Org. Biomol. Chem.
, 2023
, 21
, 2990
- An investigation into the electrophilic cyclisation of N-acyl-pyrrolidinium ions: a facile synthesis of pyrrolo-tetrahydroisoquinolones and pyrrolo-benzazepinones. Frank D. King, Abil E. Aliev, Stephen Caddick, Royston C. B. Copley
, Org. Biomol. Chem.
, 2009
, 7
, 3561
- DBSA catalyzed, one-pot three-component “on water” green protocol for the synthesis of 2,3-disubstituted 4-thiazolidinones. Davinder Prasad, Amreeta Preetam, Mahendra Nath
, RSC Adv.
, 2012
, 2
, 3133
- Aluminium triflate catalysed O-glycosidation: temperature-switched selective Ferrier rearrangement or direct addition with alcohols. D. Bradley G. Williams, Sandile B. Simelane, Henok H. Kinfe
, Org. Biomol. Chem.
, 2012
, 10
, 5636
- Development of a synthetic equivalent of α,α-dicationic acetic acid leading to unnatural amino acid derivatives via tetrafunctionalized methanes. Haruyasu Asahara, Atsushi Bonkohara, Masaya Takagi, Kento Iwai, Akitaka Ito, Kotaro Yoshioka, Shinki Tani, Kazuto Umezu, Nagatoshi Nishiwaki
, Org. Biomol. Chem.
, 2022
, 20
, 2282
- Green biorefinery — the ultra-high hydrolysis rate and behavior of Populus tomentosa hemicellulose autohydrolysis under moderate subcritical water conditions. Yanru Xu, Pengfei Wang, Shiwen Xue, Fangong Kong, Hao Ren, Huamin Zhai
, RSC Adv.
, 2020
, 10
, 18908