- In
organic chemistry,
regioselectivity is the
preference of
chemical bonding or
breaking in one
direction over all
other possible directions. It can often...
-
carbonyl ylide and on the
methyl propargyl ether terminal alkyne carbon.
Regioselectivities of 1,3-dipolar
cycloaddition reactions mediated by
metal catalysis...
-
Frontier molecular orbital theory has also been used to
explain the
regioselectivity patterns observed in Diels–Alder
reactions of
substituted systems....
-
Sharpless asymmetric dihydroxylation (also
called the
Sharpless bishydroxylation) is the
chemical reaction of an
alkene with
osmium tetroxide in the presence...
- Bystroem,
Styrbjoern E.; Nordberg, Ruth E. (November 1984). "Stereo- and
regioselective palladium-catalyzed 1,4-diacetoxylation of 1,3-dienes". The Journal...
-
charge and
creating the
final alcohol product.
Oxymercuration is very
regioselective and is a
textbook Markovnikov reaction;
ruling out
extreme cases, the...
- of
limonene is to carvone. The three-step
reaction begins with the
regioselective addition of
nitrosyl chloride across the
trisubstituted double bond...
- Interscience. pp. 350–352. Zimmerman, H. E.; Wang, P. A. (1990). "The
Regioselectivity of the
Birch Reduction". J. Am. Chem. Soc. 112 (3): 1280–1281. doi:10...
-
increased reactions rates compared to
smaller rings in SN1 reactions. The
regioselectivity of
water elimination is
highly influenced by ring size. When water...
- Earlier, the same
research group also
delineated the
rules surrounding regioselectivities ****ociated with
adding nucleophiles to
pyridinium electrophiles with...
