Enantioselectivity in the boron aldol reactions of methyl ketones.
DFT computed transition states quantitatively explain the surprising stereochemical outcome of unsubstituted enolborinates in diastereoselective and enantioselective boron aldol reactions.
Κύριοι συγγραφείς: | Goodman, J, Paton, R |
---|---|
Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
Royal Society of Chemistry
2007
|
Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
-
Understanding the origins of remote asymmetric induction in the boron aldol reactions of beta-alkoxy methyl ketones.
ανά: Paton, R, κ.ά.
Έκδοση: (2006) -
1,5-anti stereocontrol in the boron-mediated aldol reactions of beta-alkoxy methyl ketones: the role of the formyl hydrogen bond.
ανά: Paton, R, κ.ά.
Έκδοση: (2008) -
Histidine-based copper tetrapeptides as enantioselective catalysts for aldol reactions
ανά: Begum, Sharifa Zaithun, κ.ά.
Έκδοση: (2018) -
Enantioselective organocatalytic aldol reaction of ynones and its synthetic applications.
ανά: Silva, F, κ.ά.
Έκδοση: (2006) -
Carbene-catalyzed enantioselective aldol reaction : post-aldol stereochemistry control and formation of quaternary stereogenic centers
ανά: Yang, Xing, κ.ά.
Έκδοση: (2021)