Navigation

0 Hits

  • Previous / Next

You are using Science Of Synthesis as a Guest.
Please login to access the full content or check if you have access via
26.6.3.1.1.10 Variation 10: Bromination with Bromine Donors: Hexabromocyclopentadiene and ­Bromomalonic Derivatives

DOI: 10.1055/sos-SD-026-00761

Suffert, J.Science of Synthesis, (200526916.

Hexabromocyclopentadiene 148 readily brominates ketones at the α-position (Scheme 66). It usually provides the most thermodynamically stable bromo derivative, although kinetically controlled products are sometimes observed before isomerization occurs.[‌150‌]

Meeeee 88 α-Meeeeeeeeee ee Meeeeee Meeee Meeeeeeeeeeeeeeeeeeeeeee[‌888‌]

M eeeeeee eeeeeee ee 8,8-eeeeeee-8,8-eeeeeeee-8,8-eeeeeee-8,8-eeeee (888), e eeeeeeeee eeeee, eeeeee eee eeeeee ee 8°M; ee eeeeeeeeee eeeeeeeee eeeeeee ee eee eeee eeeeeeeeeee α-eeeeeeee (Meeeee 88).[‌888‌] Me eee eeeeeeee eeeeee ee eeee eeeeeeeeeee eee ee eeeeeeee ee eeeeeeee eeee eeeeeeeee, eeeeeeee eeeeeeeee eeee e eeeeeee eeeeee ee eee eeeeeee, eee ee eeeeee eee eee eeeeeeeeeee ee eeeeeeeee eeeeeee; eeeeeeee, eee α-eeeeeeeeee eeeeeee 888 ee eeeeee eeeeeeee ee eeeeeee eeee eee eeeeeeeee, Meeeeee'e eeee, eeee ee eeeeeee eeeeeeee ee eeeeee eeeeeeee eeeeeeeee.

Meeeee 88 α-Meeeeeeeeee ee e Meeeee Meeee 8,8-Meeeeee-8,8-eeeeeeee-8,8-eeeeeee-8,8-eeeee[‌888‌]

References


Cookie-Einstellungen