Reagent-Controlled α-Selective Dehydrative Glycosylation of 2,6-Dideoxy- and 2,3,6-Trideoxy Sugars.
about
Mild Method for 2-Naphthylmethyl Ether Protecting Group Removal Using a Combination of 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) and β-Pinene.Palladium-Catalyzed Direct Stereoselective Synthesis of Deoxyglycosides from GlycalsCooperative Brønsted Acid-Type Organocatalysis for the Stereoselective Synthesis of Deoxyglycosides.Dehydrative glycosylation with cyclic phosphonium anhydrides.Gold(I)-Catalyzed Direct Stereoselective Synthesis of Deoxyglycosides from Glycals.Comprehensive review of chemical strategies for the preparation of new aminoglycosides and their biological activities.
P2860
Reagent-Controlled α-Selective Dehydrative Glycosylation of 2,6-Dideoxy- and 2,3,6-Trideoxy Sugars.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh-hant
name
Reagent-Controlled α-Selective ...... xy- and 2,3,6-Trideoxy Sugars.
@en
Reagent-Controlled α-Selective ...... xy- and 2,3,6-Trideoxy Sugars.
@nl
type
label
Reagent-Controlled α-Selective ...... xy- and 2,3,6-Trideoxy Sugars.
@en
Reagent-Controlled α-Selective ...... xy- and 2,3,6-Trideoxy Sugars.
@nl
prefLabel
Reagent-Controlled α-Selective ...... xy- and 2,3,6-Trideoxy Sugars.
@en
Reagent-Controlled α-Selective ...... xy- and 2,3,6-Trideoxy Sugars.
@nl
P2093
P2860
P356
P1476
Reagent-Controlled α-Selective ...... oxy- and 2,3,6-Trideoxy Sugars
@en
P2093
Danielle K Bright
Jason M Nogueira
Marissa Bylsma
P2860
P304
10088-10092
P356
10.1002/ANIE.201605091
P407
P577
2016-07-19T00:00:00Z