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- Bioinspired design for the assembly of Glypromate® neuropeptide conjugates with active pharmaceutical ingredients. Sara C. Silva-Reis, A. Catarina V. D. dos Santos, Xerardo García-Mera, José E. Rodríguez-Borges, Ivo E. Sampaio-Dias
, New J. Chem.
, 2020
, 44
, 21049
- Expeditious synthesis of 1-aminoindane derivatives achieved by [1,4]-hydride shift mediated C(sp3)–H bond functionalization. Keiji Mori, Kazuki Kurihara, Takahiko Akiyama
, Chem. Commun.
, 2014
, 50
, 3729
- Selective derivatisation of resorcarenes: Part 7. The reason for the diastereoselectivity of Mannich reactions with chiral amines. Christian Schmidt, Erich F. Paulus, Volker Böhmer, Walter Vogt
, New J. Chem.
, 2001
, 25
, 374
- R-VAPOL-phosphoric acid based 1H and 13C-NMR for sensing of chiral amines and acids. Durga Prasad, Santosh Mogurampelly, Sachin R. Chaudhari
, RSC Adv.
, 2020
, 10
, 2303
- Overcoming a solid solution system on chiral resolution: combining crystallization and enantioselective dissolution. Ryusei Oketani, Koki Shiohara, Ichiro Hisaki
, Chem. Commun.
, 2023
, 59
, 6175
- Recyclable silica-supported prolinamide organocatalysts for direct asymmetric Aldol reaction in water. Amàlia Monge-Marcet, Xavier Cattoën, Diego A. Alonso, Carmen Nájera, Michel Wong Chi Man, Roser Pleixats
, Green Chem.
, 2012
, 14
, 1601
- Structural features localizing the ferroptosis inhibitor GIF-2197-r to lysosomes. Yoko Hirata, Tomohiro Hashimoto, Kaori Ando, Yuji O. Kamatari, Hiroshi Takemori, Kyoji Furuta
, RSC Adv.
, 2023
, 13
, 32276
- RES-TOCSY: a simple approach to resolve overlapped 1H NMR spectra of enantiomers. Lokesh, Sachin Rama Chaudhari, N. Suryaprakash
, Org. Biomol. Chem.
, 2014
, 12
, 993
- Systematic study of steric and spatial contributions to molecular recognition by non-covalent imprinted polymers. David A. Spivak, Jason Campbell
, Analyst
, 2001
, 126
, 793
- Enantioselective synthesis of 1-aminoindene derivatives via asymmetric Brønsted acid catalysis. Xiang Wu, Du Ding, Ying Zhang, Hua-Jie Jiang, Tao Wang, Li-Ping Zhao
, Chem. Commun.
, 2021
, 57
, 9680