An Expeditious Synthesis of Sialic Acid Derivatives by Copper(I)-Catalyzed Stereodivergent Propargylation of Unprotected Aldoses.
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Enantioselective copper catalysed, direct functionalisation of allenes via allyl copper intermediates.Enantioselective Generation of Adjacent Stereocenters in a Copper-Catalyzed Three-Component Coupling of Imines, Allenes, and DiboranesC-Propargylation Overrides O-Propargylation in Reactions of Propargyl Chloride with Primary Alcohols: Rhodium-Catalyzed Transfer Hydrogenation.Synthesis of sialic acid derivatives based on chiral substrate-controlled stereoselective aldol reactions using pyruvic acid oxabicyclo[2.2.2]octyl orthoester.Stereodivergent Synthesis of Functionalized Tetrahydropyrans Accelerated by Mechanism-Based Allylboration and Bioinspired Oxa-Michael Cyclization.
P2860
An Expeditious Synthesis of Sialic Acid Derivatives by Copper(I)-Catalyzed Stereodivergent Propargylation of Unprotected Aldoses.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
An Expeditious Synthesis of Si ...... lation of Unprotected Aldoses.
@en
type
label
An Expeditious Synthesis of Si ...... lation of Unprotected Aldoses.
@en
prefLabel
An Expeditious Synthesis of Si ...... lation of Unprotected Aldoses.
@en
P2860
P1433
P1476
An Expeditious Synthesis of Si ...... lation of Unprotected Aldoses.
@en
P2093
Motomu Kanai
Xiao-Feng Wei
P2860
P356
10.1021/ACSCENTSCI.5B00360
P577
2016-01-04T00:00:00Z