-
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...
-
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...
-
imines but more
reactive towards nucleophiles. A
nucleophile adds
diastereoselectively over the
imine group in an
electrophilic addition with the tert-butanesulfinyl...
- and formaldehyde, the
Prins reaction. 1,3-diols can be
produced diastereoselectively from the
corresponding β-hydroxy
ketones using the Evans–Saksena...
- 15227/orgsyn.081.0157. Dondoni, Alessandro; Perrone,
Daniela (2000). "
Diastereoselective Synthesis of
Protected Vicinal Amino Alcohols: (S)-2-[(4s)-n-tert-butoxycarbonyl-2...
- 1021/ol062112m. PMID 17078705.
Varin M, Barré E,
Iorga B,
Guillou C (2008). "
Diastereoselective total synthesis of (+/-)-codeine". Chemistry: A
European Journal....
- Denichoux, Aurélien; Chemla, Fabrice; Bejjani,
Joseph (2004). "Highly
Diastereoselective Syntheses of
Propargylic Acid and
Homopropargylic Systems". Synlett...
- ISBN 978-0-12-800807-2. Gage,
James R.; Evans,
David A. (1990). "
Diastereoselective Aldol Condensation Using a
Chiral Oxazolidinone Auxiliary: (2S...
- The
Michael addition is an
important atom-economical
method for
diastereoselective and
enantioselective C–C bond formation, and many
asymmetric variants...
