-
galactose to be
absorbed slightly faster than
glucose in
human body.
Diastereoselectivity is the
preference for the
formation of one or more than one diastereomer...
- the substrate; second, the
resulting compound undergoes one or more
diastereoselective transformations; and finally, the
auxiliary is
removed under conditions...
- Furthermore,
enantiomeric purity can be
achieved by
hydrogenation of the
diastereoselective product.
Apart from amino-acids, PBM
reaction can also be used to...
-
reaction would also be
called diastereoselective. Cram's rule
predicts the
major diastereomer resulting from the
diastereoselective nucleophilic addition to...
-
produced by a
multistep route from 3-amino-1-propanol. Regio- and
diastereoselective synthesis of 2-arylazetidines
could be
performed from appropriately...
- Narasaka–Prasad reduction,
sometimes simply called Narasaka reduction, is a
diastereoselective reduction of β-hydroxy
ketones to the
corresponding syn-dialcohols...
-
hydride source Zn(BH4)2 also
shows 1,2 selectivity, as well as
greater diastereoselectivity. It does so by
coordinating not only to the
carbonyl oxygen but also...
- ISBN 978-0-12-800807-2. Gage,
James R.; Evans,
David A. (1990). "
Diastereoselective Aldol Condensation Using a
Chiral Oxazolidinone Auxiliary: (2S...
-
David A.; Tedrow,
Jason S.; Shaw,
Jared T.; Downey, C. Wade (2002). "
Diastereoselective Magnesium Halide-Catalyzed anti-Aldol
Reactions of
Chiral N-Acyloxazolidinones"...
- The
Michael addition is an
important atom-economical
method for
diastereoselective and
enantioselective C–C bond formation, and many
asymmetric variants...
