-
galactose to be
absorbed slightly faster than
glucose in the
human body.
Diastereoselectivity is the
preference for the
formation of one or more than one diastereomer...
- In 2013,
Carreira and co-workers
reported a
highly enantio- and
diastereoselective α-allylation of
branched aldehydes. They used
chiral primary amines...
- 1002/047084289X.rc041.pub3. ISBN 9780471936237. Greeves, Nick (2015). "
Diastereoselective Ketone Reduction". ChemTube3D.
University of Liverpool. Retrieved...
- The Saksena–Evans
reduction is a
diastereoselective reduction of β-hydroxy
ketones to the
corresponding anti-dialcohols,
employing the
reagent tetramethylammonium...
-
reaction would also be
called diastereoselective. Cram's rule
predicts the
major diastereomer resulting from the
diastereoselective nucleophilic addition to...
-
Protected at the
aldehyde function with (R)-BINOL,
arylglyoxals reacted diastereoselectively with
Grignard reagents to
afford protected atrolactaldehyde with...
- The
Michael addition is an
important atom-economical
method for
diastereoselective and
enantioselective C–C bond formation, and many
asymmetric variants...
-
diastereoselection in 1,3-dipolar cycloaddition.
Examples of substrate-controlled
diastereoselective 1,3-dipolar
cycloadditions are
shown below.
First is the reaction...
- and formaldehyde, the
Prins reaction. 1,3-diols can be
produced diastereoselectively from the
corresponding β-hydroxy
ketones using the Evans–Saksena...
- 1021/ol062112m. PMID 17078705.
Varin M, Barré E,
Iorga B,
Guillou C (2008). "
Diastereoselective total synthesis of (+/-)-codeine". Chemistry: A
European Journal....
