๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Synthesis and determination of the absolute configurations of the enantiomeric 1,2-epoxy-1-phenylcyclohexanes

โœ Scribed by Berti, Giancarlo; Macchia, Bruno; Macchia, Franco; Monti, Luigi


Book ID
118209537
Publisher
American Chemical Society
Year
1968
Tongue
English
Weight
748 KB
Volume
33
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Synthesis and assignment of absolute con
โœ Boลผenna Krzyลผanowska; Wojciech J. Stec; Michaล‚ W. Wieczorek; Jarosล‚aw Bล‚aszczyk ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 604 KB

## Abstract The title compound __2__ has been synthesized and its structure has been determined by Xโ€ray analysis. The following crystal data were found: monoclinic, P2~1~, a = 9.936(4), b = 18.009(3), c = 10.418(3) ร…, and ฮฒ = 107.22(3)ยฐ. Two molecules of the compound (two oxathiaphospholane anions

Determination of absolute configuration
โœ Kuninobu Kabuto; Fujiko Yasuhara; Shozo Yamaguchi ๐Ÿ“‚ Article ๐Ÿ“… 1984 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 265 KB

Absolute configuration and enantiomeric purities of some hydroxyketones and diols of spiro[4\_4]nonane and 2,2'-spirobi-indan can be simultaneously determined by use of MTPA derivatives and a lanthanoid shift reagent.

NMR determination of the absolute config
โœ Hiroki Fukui; Yukiharu Fukushi; Satoshi Tahara ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 218 KB

Each of the chiral 1,2-and 1,3-diols examined was derivatized exclusively to a single diastereomeric acetal by the use of a new axially chiral reagent, 2%-methoxy-1,1%-binaphthalene-8-carbaldehyde (MBC). The absolute configuration of the original 1,2-and 1,3-diols was determined by the NOE correlati

Correlation of the Absolute Configuratio
โœ Univ.-Doz. Dr. Volker Schurig; Bernhard Koppenhรถfer; Waldemar Bรผrkle ๐Ÿ“‚ Article ๐Ÿ“… 1978 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 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