Synthesis and determination of the absolute configurations of the enantiomeric 1,2-epoxy-1-phenylcyclohexanes
โ 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.
๐ SIMILAR VOLUMES
## Abstract The title compound __2__ has been synthesized and its structure has been determined by Xโray 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
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.
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
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