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- Applications of oxazolidinones as chiral auxiliaries in the asymmetric alkylation reaction applied to total synthesis. Majid M. Heravi, Vahideh Zadsirjan, Behnaz Farajpour
, RSC Adv.
, 2016
, 6
, 30498
- Asymmetric Diels–Alder reaction of 3-(acyloxy)acryloyl oxazolidinones: optically active synthesis of a high-affinity ligand for potent HIV-1 protease inhibitors. Arun K. Ghosh, Alessandro Grillo, Satish Kovela, Margherita Brindisi
, RSC Adv.
, 2019
, 9
, 41755
- Optimum operating conditions for chiral separations in liquid chromatography. R. P. W. Scott, Thomas E. Beesley
, Analyst
, 1999
, 124
, 713
- The enantioselective total syntheses of (+)-7-oxohinokinin, (+)-7-oxoarcitin, (+)-conicaol B and (−)-isopolygamain. Emily K. Paulin, Euphemia Leung, Lisa I. Pilkington, David Barker
, Org. Biomol. Chem.
, 2022
, 20
, 4324
- Highly stereoselective gram scale synthesis of all the four diastereoisomers of Boc-protected 4-methylproline carboxylates. Kehuan Sun, Cheng Tao, Bohua Long, Xiaobin Zeng, Zhengzhi Wu, Ronghua Zhang
, RSC Adv.
, 2019
, 9
, 32017
- Synthesis and medicinal chemistry of selected antitubercular natural products and natural product derivatives. Aman Mahajan, Renate Hans, Kelly Chibale, Vipan Kumar
, RSC Adv.
, 2014
, 4
, 15180
- Structure determination, correction, and disproof of marine macrolide natural products by chemical synthesis. Haruhiko Fuwa
, Org. Chem. Front.
, 2021
, 8
, 3990
- Total synthesis of amphidinins E, F and epi-amphidinin F. Kai Chen, Zhengshuang Xu, Tao Ye
, Org. Chem. Front.
, 2018
, 5
, 629
- Helix-forming aliphatic homo-δ-peptide foldamers based on the conformational restriction effects of cyclopropane. Makoto Nagata, Mizuki Watanabe, Ryohei Doi, Mai Uemura, Nanase Ochiai, Wataru Ichinose, Koichi Fujiwara, Yoshihiro Sato, Tomoshi Kameda, Koh Takeuchi, Satoshi Shuto
, Org. Biomol. Chem.
, 2023
, 21
, 970
- β3R3-Peptides: design and synthesis of novel peptidomimetics and their self-assembling properties at the air–water interface. Simone Mosca, Claudia Dannehl, Uwe Möginger, Gerald Brezesinski, Laura Hartmann
, Org. Biomol. Chem.
, 2013
, 11
, 5399