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Synthese d'hydroxy-2 esters enantiomeriquement purs a partir d'amino-2 acide : etude stereochimique de l'addition 1,4 d'organometalliques sur des systemes insatures-2,3 hydroxy-4
FR |
EN
| Auteur / Autrice : | YVES PETIT |
| Direction : | Marc Larchevêque |
| Type : | Thèse de doctorat |
| Discipline(s) : | Chimie |
| Date : | Soutenance en 1987 |
| Etablissement(s) : | Paris 6 |
Mots clés
FR
Mots clés libres
Chimie
Chimie organique
Insecta
Arthropoda
Invertebrata
Induction asymetrique
Exces enantiomere
Alcool
Heterocycle oxygene
Cycle 5 chainons
Pheromone sexuelle
Aminoacide
Cetol
Compose allylique
Lithium compose organique
Lepidoptera
Condensation chimique
Magnesium cuivre compose organique
Pyralidae
Desamination nitreuse
Eldana saccharina
Eldanolide|fin
Aspartique acide derive|ent
Serine derive|ent
Oxirannecarboxylique acide,ester alkyle|ent
Propionique acide(bromo-2 hydroxy-3)
Malonique acide derive
Enantiospecificite
Furanne derive
Hydroxy ester
Pseudococcus comstockue
Aldol
Lactone
Insecta
Arthropoda
Invertebrata
Asymmetric induction
Enantiomeric excess
Alcohol
Oxygen heterocycle
Five membered ring
Sex pheromone
Aminoacid
Ketol
Allylic compound
Lithium organic compounds
Lepidoptera
Condensation reaction
Magnesium copper organic compounds
Pyralidae
Nitrous deamination
Eldana saccharina
Résumé
FR
Application de cette addition a la synthese d'eldanolide