Convenient Catalytic Synthesis and Assignment of the Absolute Configuration of Enantiomerically Pure Dihydronaphthalenes and Their Corresponding Epoxides. -The asymmetric epoxidation of known dihydronaphthalene derivative (I) is investigated in order to obtain enantiomerically pure epoxide (II), ne
✦ LIBER ✦
Convenient Catalytic Synthesis and Assignment of the Absolute Configuration of Enantiomerically Pure Dihydronaphthalenes and Their Corresponding Epoxides
✍ Scribed by Torsten Linker; Frank Rebien; Gábor Tóth; András Simon; Jürgen Kraus; Gerhard Bringmann
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 195 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0947-6539
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
ChemInform Abstract: Convenient Catalyti
✍
T. LINKER; F. REBIEN; G. TOTH; A. SIMON; J. KRAUS; G. BRINGMANN
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 31 KB
👁 2 views
ChemInform Abstract: The First Synthesis
✍
Guoqiang Lin; Aimin Zhang
📂
Article
📅
2010
🏛
John Wiley and Sons
⚖ 27 KB
👁 2 views
Correlation of the Absolute Configuratio
✍
Univ.-Doz. Dr. Volker Schurig; Bernhard Koppenhöfer; Waldemar Bürkle
📂
Article
📅
1978
🏛
John Wiley and Sons
🌐
English
⚖ 312 KB
is therefore generated in situ from trichloroacetohydroximoyl chloride (4)['l. While oxepin reacts directly with ( 1 ) to give (3), reaction of ( 1 ) with 1,3-cyclohexadiene gives cycloadduct ( 5 ) as intermediate. This thermally labile compound rearranges even at room temperature, and more rapidly