Highly Enantioselective Isomerization of 4,7-Dihydro-1,3-dioxepins Catalyzed by Me-DuPHOS-Modified Dihalogenonickel Complexes and Determination of the Absolute Configuration of the Isomerization Products This work was supported by the Fonds der Chem
about
Highly Enantioselective Isomerization of 4,7-Dihydro-1,3-dioxepins Catalyzed by Me-DuPHOS-Modified Dihalogenonickel Complexes and Determination of the Absolute Configuration of the Isomerization Products This work was supported by the Fonds der Chem
description
2001 nî lūn-bûn
@nan
2001 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Highly Enantioselective Isomer ...... upported by the Fonds der Chem
@ast
Highly Enantioselective Isomer ...... upported by the Fonds der Chem
@en
type
label
Highly Enantioselective Isomer ...... upported by the Fonds der Chem
@ast
Highly Enantioselective Isomer ...... upported by the Fonds der Chem
@en
prefLabel
Highly Enantioselective Isomer ...... upported by the Fonds der Chem
@ast
Highly Enantioselective Isomer ...... upported by the Fonds der Chem
@en
P2093
P1433
P1476
Highly Enantioselective Isomer ...... upported by the Fonds der Chem
@en
P2093
Dirk Brethauer
Gerhard Raabe
Herbert Frauenrath
Martin Maurer
Stefan Reim
P304
P356
10.1002/1521-3773(20010105)40:1<177::AID-ANIE177>3.3.CO;2-O
P577
2001-01-01T00:00:00Z