-
important electrophiles are aldehydes/ketones and
Michael acceptors.
Regiospecific formation is the
controlled enolate formation by the
specific deprotonation...
- In
organic chemistry,
regioselectivity is the
preference of
chemical bonding or
breaking in one
direction over all
other possible directions. It can often...
-
atoms in this
phosphate ester are differentiated,
setting the
stage for
regiospecific formation of triglycerides, as the diol
reacts selectively with coenzyme-A...
-
vinylidene fluoride (VF2), however, the
polymerization is not
completely regiospecific. The
asymmetric structure of VF2
leads to the
orientation isomers during...
-
Adams J,
Schulte GR,
Chesworth R,
Miyazaki Y, et al. (August 2009). "
Regiospecific and
stereoselective syntheses of (+/-) morphine, codeine, and thebaine...
-
Regiospecific hydroboration with borane...
- chloride: The
diene has two
features of interest: the
substituents promote regiospecific addition to
unsymmetrical dienophiles and the
resulting adduct is amenable...
- 1016/S0040-4020(01)85435-1. Zhou, Hao; Liao, Xuebin; Cook,
James M. (2004-01-01). "
Regiospecific,
Enantiospecific Total Synthesis of the 12-Alkoxy-Substituted Indole...
- 4-****tones by the
reaction of
silyl enol
ether with
silver oxide.
Regiospecific formation of silver(I)
enolate intermediates".
Journal of the American...
- ISBN 978-3-88763-075-1.
Numazawa M,
Nagaoka M,
Kunitama Y (September 1986). "
Regiospecific deoxygenation of the
dihydroxyacetone moiety at C-17 of
corticoid steroids...
