๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Trans-coplanar rearrangements: the synthesis of trans- and cis-bicyclo[7.1.0]decan-2-one

โœ Scribed by Joseph V. Paukstelis; Jar-Lin Kao

Publisher
Elsevier Science
Year
1970
Tongue
French
Weight
162 KB
Volume
11
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

The synthesis of cis- and trans-1,2-dibr
The synthesis of cis- and trans-1,2-dibromocyclopropane
โœ J.W.F.L. Seetz; O.S. Akkerman; F. Bickelhaupt ๐Ÿ“‚ Article ๐Ÿ“… 1981 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 129 KB

A preparative route to cis-and trans-1,2-dibromocyclopropane ' Trans-& b.p. (120ยฐC/300 mbar) and H NMR spectrum were In agreement with the literature 2 ; w m.p. 8OC; b.p. 120ยฐC/100 mbar; 'H NMR spectrum (CDC13, 250 Mhz): 6 = 3.10 ppm (dd,

Stereochemistry of the rearrangement of
Stereochemistry of the rearrangement of cis- and trans-1,2-divinyl-1,2-cyclohexanediols
โœ Elliot N. Marvell; William Whalley ๐Ÿ“‚ Article ๐Ÿ“… 1969 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 178 KB

Rearrangement of 1,2-divinyl-1,2-cyclohexanediol (I) was shown by Coda, et al (1) to give l-bicyclo[5.3.O]decen-2-one (II). We had made the ssme observation independently (2), but had also found that under milder conditions 7-hydroxybicyclo[5.3,0] decsn-2-one (III) can be isolated in good yield. In