A convenient, one-step synthesis of optically active tertiary aminonaphthol and its applications in the highly enantioselective alkenylations of aldehydes.

A convenient, one-step synthesis of optically active tertiary aminonaphthol and its applications in the highly enantioselective alkenylations of aldehydes.

Item
http://www.wikidata.org/entity/Q44314519
Mannich bases: an important pharmacophore in present scenarioActivation of vinyl iodides for the highly enantioselective addition to aldehydes.Formation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition of Carbonyl Compounds and IminesCatalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents.Enantioselective iridium-catalyzed carbonyl allylation from the alcohol oxidation level via transfer hydrogenation: minimizing pre-activation for synthetic efficiencyFormation of C-C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation.Recent developments in asymmetric multicomponent reactions.Catalytic asymmetric synthesis of allylic alcohols and derivatives and their applications in organic synthesis.Direct vinylation of alcohols or aldehydes employing alkynes as vinyl donors: a ruthenium catalyzed C-C bond-forming transfer hydrogenation.Formation of C-C Bonds via Ruthenium Catalyzed Transfer Hydrogenation: Carbonyl Addition from the Alcohol or Aldehyde Oxidation LevelCatalytic enantioselective synthesis of α-substituted secondary allylic alcohols from terminal alkynes and aldehydes via vinylaluminum reagents.Synthesis of P-Stereogenic Phosphoramidite and Phosphorodiamidite Ligands and Their Application in Asymmetric Catalysis
P2860

A convenient, one-step synthesis of optically active tertiary aminonaphthol and its applications in the highly enantioselective alkenylations of aldehydes.

Item
http://www.wikidata.org/entity/Q44314519
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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@zh-hans
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name
A convenient, one-step synthes ...... ve alkenylations of aldehydes.
@en
A convenient, one-step synthes ...... ve alkenylations of aldehydes.
@nl
type
label
A convenient, one-step synthes ...... ve alkenylations of aldehydes.
@en
A convenient, one-step synthes ...... ve alkenylations of aldehydes.
@nl
prefLabel
A convenient, one-step synthes ...... ve alkenylations of aldehydes.
@en
A convenient, one-step synthes ...... ve alkenylations of aldehydes.
@nl
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P577
P698
P921
P356
P1433
P1476
A convenient, one-step synthes ...... ve alkenylations of aldehydes.
@en
P2093
P304
P31
P356
P407
P433
P478
P577
P698
P921