Tungsten-catalyzed regioselective and stereospecific ring opening of 2,3-epoxy alcohols and 2,3-epoxy sulfonamides.
about
Tungsten-catalyzed regio- and enantioselective aminolysis of trans-2,3-epoxy alcohols: an entry to virtually enantiopure amino alcoholsGadolinium-Catalyzed Regio- and Enantioselective Aminolysis of Aromatic trans-2,3-Epoxy Sulfonamides.Synthesis of virtually enantiopure aminodiols with three adjacent stereogenic centers by epoxidation and ring-opening.A Migratory Ether Formation Route to Medium-Sized Sugar Mimetics.Synthesis of a highly reactive form of WO2Cl2, its conversion into nanocrystalline mono-hydrated WO3 and coordination compounds with tetramethylurea.
P2860
Tungsten-catalyzed regioselective and stereospecific ring opening of 2,3-epoxy alcohols and 2,3-epoxy sulfonamides.
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Tungsten-catalyzed regioselect ...... ls and 2,3-epoxy sulfonamides.
@ast
Tungsten-catalyzed regioselect ...... ls and 2,3-epoxy sulfonamides.
@en
type
label
Tungsten-catalyzed regioselect ...... ls and 2,3-epoxy sulfonamides.
@ast
Tungsten-catalyzed regioselect ...... ls and 2,3-epoxy sulfonamides.
@en
prefLabel
Tungsten-catalyzed regioselect ...... ls and 2,3-epoxy sulfonamides.
@ast
Tungsten-catalyzed regioselect ...... ls and 2,3-epoxy sulfonamides.
@en
P2860
P356
P1476
Tungsten-catalyzed regioselect ...... ls and 2,3-epoxy sulfonamides.
@en
P2093
Hisashi Yamamoto
P2860
P304
P356
10.1021/JA5029809
P407
P50
P577
2014-05-02T00:00:00Z