Unknown

Dataset Information

0

Efficient synthesis of dipeptide analogues of α-fluorinated β-aminophosphonates.

ABSTRACT: Herein, we present an efficient synthesis of dipeptide analogues of α-fluorinated β-aminophosphonates. Each step of the synthesis was optimized to provide excellent yields. Moreover, the absolute configuration of the obtained compounds was determined by X-ray analysis, which proved the stereochemistry that was proposed based on NMR studies.

SUBMITTER: Kazmierczak M 

PROVIDER: S-EPMC7176923 | biostudies-literature |

REPOSITORIES: biostudies-literature

Json Xml

Similar Datasets

Unknown Efficient Synthesis of New Fluorinated β-Amino Acid Enantiomers through Lipase-Catalyzed Hydrolysis.
| S-EPMC7766834 | biostudies-literature
Unknown Kinetics and mechanism of inhibition of serine esterases by fluorinated aminophosphonates.
| S-EPMC4820331 | biostudies-other
Unknown Synthesis of mixed opioid affinity cyclic endomorphin-2 analogues with fluorinated phenylalanines.
| S-EPMC4434475 | biostudies-literature
Unknown Design, Synthesis, and Anti-RNA Virus Activity of 6'-Fluorinated-Aristeromycin Analogues.
| S-EPMC7075649 | biostudies-literature
Unknown Catalyst-Free Cross-Dehydrogenative Coupling Strategy Using Air as an Oxidant: Synthesis of α-Aminophosphonates.
| S-EPMC6641911 | biostudies-literature
Unknown Ugi Reaction on α-Phosphorated Ketimines for the Synthesis of Tetrasubstituted α-Aminophosphonates and Their Applications as Antiproliferative Agents.
| S-EPMC8002371 | biostudies-literature
Unknown Modular synthesis of α-fluorinated arylmethanes via desulfonylative cross-coupling.
| S-EPMC6778098 | biostudies-literature
Unknown Potent fluorinated agelastatin analogues for chronic lymphocytic leukemia: design, synthesis, and pharmacokinetic studies.
| S-EPMC4079331 | biostudies-literature
Unknown Efficient, divergent synthesis of cryptophycin unit A analogues.
| S-EPMC3494784 | biostudies-literature
Unknown Synthesis, Stability, and Biological Studies of Fluorinated Analogues of Thromboxane A<sub>2</sub>.
| S-EPMC7318075 | biostudies-literature