about
LiOOt-Bu as a terminal oxidant in a titanium alkoxide-mediated [2+2+2] reaction cascade.Electrophilic amination: the case of nitrenoids.Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres.Regio- and stereoselective monoepoxidation of dienes using methyltrioxorhenium: synthesis of allylic epoxidesSynthesis of Ethers via Reaction of Carbanions and Monoperoxyacetals.Enantioselective Construction of Acyclic Quaternary Carbon Stereocenters: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Amide Enolates.Stereodefined acyclic trisubstituted metal enolates towards the asymmetric formation of quaternary carbon stereocentres.Mononuclear Alkali Metal Organoperoxides Stabilized by an NNNN-Macrocycle and Short Hydrogen Bonds from ROOH Molecules.Asymmetric Catalytic Preparation of Polysubstituted Cyclopropanol and Cyclopropylamine Derivatives.Brook Rearrangement as a Trigger for the Ring Opening of Strained Carbocycles.
P2860
Q35747699-31A2E61B-AFEA-485F-BFBA-1C429D97774DQ38340331-E8BA993A-AFA8-4C51-96C7-D16F5EE05455Q41833646-5B31A378-C536-4F16-A829-FE135543F1ECQ42262505-E2D86F6E-B2FB-48A6-AAD6-15D73B4C9134Q43119887-949DCE07-61D1-4ED5-97B8-1FF1CEFDAC61Q46642667-79198399-6BA8-4B15-AB6A-7B4ED3E52436Q46862564-1A693BCE-0ED8-47ED-A599-BE0D02BAB674Q48105400-4AAB0512-FA9B-4A7B-BF71-75FC692C5410Q48269544-3E39D121-0731-4932-823D-ED15E0BA0CADQ52895598-C1F3A927-D2C6-430D-9512-8843584E929E
P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Oxenoids in organic synthesis.
@en
type
label
Oxenoids in organic synthesis.
@en
prefLabel
Oxenoids in organic synthesis.
@en
P2860
P356
P1476
Oxenoids in organic synthesis
@en
P2093
Ilan Marek
P2860
P304
P356
10.1039/C3OB42349B
P50
P577
2014-03-01T00:00:00Z