Phosphorus Chemistry I: Asymmetric Synthesis and Bioactive CompoundsJean-Luc Montchamp Springer, 6 бер. 2015 р. - 242 стор. Each review within the volume critically surveys one aspect of that topic and places it within the context of the volume as a whole. The most significant developments of the last 5 to 10 years are presented using selected examples to illustrate the principles discussed. The coverage is not intended to be an exhaustive summary of the field or include large quantities of data, but should rather be conceptual, concentrating on the methodological thinking that will allow the non-specialist reader to understand the information presented. Contributions also offer an outlook on potential future developments in the field. |
Зміст
| 1 | |
Synthesis and Biological Applications of Phosphinates and Derivatives | 39 |
Crossing the Membrane Barrier | 115 |
Recent Advances in Asymmetric Synthesis of Stereogenic Phosphorus Compounds | 161 |
| 237 | |
Інші видання - Показати все
Phosphorus Chemistry I: Asymmetric Synthesis and Bioactive Compounds Jean-Luc Montchamp Попередній перегляд недоступний - 2015 |
Phosphorus Chemistry I: Asymmetric Synthesis and Bioactive Compounds Jean-Luc Montchamp Попередній перегляд недоступний - 2016 |
Phosphorus Chemistry I: Asymmetric Synthesis and Bioactive Compounds Jean-Luc Montchamp Попередній перегляд недоступний - 2015 |
Загальні терміни та фрази
activity acyclic afforded agonists alkyl amino analogues antiviral aryl asymmetric asymmetric synthesis Balzarini benzyl BH3 BH3 bioisostere Biol biological Bioorg Med Chem bisphosphonates boranes Bu-t carboxylic catalyzed cell Chem Lett Chem Soc chemistry chiral cidofovir cleavage CO2Et CO2H complex compounds configuration cyclic deprotection derivatives diastereomers diastereoselective diphosphate diphosphine Dive drug ee Scheme enantiomeric enantiomers enantiopure enantioselectivity enzymatic enzyme ester Et3N evaluation formation fosmidomycin GABA Georgiadis glutamate H-phosphinic H₂N hydrogenation hydrolysis i-Pr inhibition interactions isoprenoid ligands lipase Matziari MeOH metabolism methyl Michael addition nucleoside OH OH oxides P-chirogenic P-stereogenic peptide Ph Ph phenyl phosphate phosphine boranes phosphinic acid phosphinic peptides phosphinite phosphoramidate phosphorus phosphorus atom phosphoryl prepared prodrugs proteases protecting groups protein pseudodipeptides racemic reaction receptor reflux secondary phosphines selective stereoselectivity strategy structure substrate synthetic t-Bu target tertiary phosphines Tetrahedron toluene virus vitro Yiotakis