115 related articles for article (PubMed ID: 22235771)
1. The role of β-bulky substituents in aldol reactions of boron enolates of methylketones with aldehydes: experimental and theoretical studies by DFT analysis.
Dias LC; de Lucca EC; Ferreira MA; Garcia DC; Tormena CF
J Org Chem; 2012 Feb; 77(4):1765-88. PubMed ID: 22235771
[TBL] [Abstract][Full Text] [Related]
2. Influence of β-substituents in aldol reactions of boron enolates of β-alkoxy methylketones.
Dias LC; de Lucca EC; Ferreira MA; Garcia DC; Tormena CF
Org Lett; 2010 Nov; 12(21):5056-9. PubMed ID: 20931986
[TBL] [Abstract][Full Text] [Related]
3. 1,5-anti stereocontrol in the boron-mediated aldol reactions of beta-alkoxy methyl ketones: the role of the formyl hydrogen bond.
Paton RS; Goodman JM
J Org Chem; 2008 Feb; 73(4):1253-63. PubMed ID: 18211083
[TBL] [Abstract][Full Text] [Related]
4. 1,5-Asymmetric induction in boron-mediated aldol reactions of beta-alkoxy methylketones.
Dias LC; de Marchi AA; Ferreira MA; Aguilar AM
J Org Chem; 2008 Aug; 73(16):6299-311. PubMed ID: 18616322
[TBL] [Abstract][Full Text] [Related]
5. The influence of a beta-electron withdrawing substituent in aldol reactions of methylketone boron enolates.
Dias LC; de Marchi AA; Ferreira MA; Aguilar AM
Org Lett; 2007 Nov; 9(23):4869-72. PubMed ID: 17939677
[TBL] [Abstract][Full Text] [Related]
6. 1,5-Stereoinduction in boron-mediated aldol reactions of β,δ-bisalkoxy methylketones containing cyclic protecting groups.
Dias LC; Polo EC; Ferreira MA; Tormena CF
J Org Chem; 2012 Apr; 77(8):3766-92. PubMed ID: 22448754
[TBL] [Abstract][Full Text] [Related]
7. 1,5-asymmetric induction in boron-mediated beta-alkoxy methyl ketone aldol addition reactions.
Evans DA; Côté B; Coleman PJ; Connell BT
J Am Chem Soc; 2003 Sep; 125(36):10893-8. PubMed ID: 12952469
[TBL] [Abstract][Full Text] [Related]
8. 1,5-Asymmetric induction in boron-mediated aldol reactions of beta-oxygenated methyl ketones.
Dias LC; Aguilar AM
Chem Soc Rev; 2008 Mar; 37(3):451-69. PubMed ID: 18224256
[TBL] [Abstract][Full Text] [Related]
9. Diastereoselectivity in the boron aldol reaction of α-alkoxy and α,β-bis-alkoxy methyl ketones.
Fernandes AAG; Leonarczyk IA; Ferreira MAB; Dias LC
Org Biomol Chem; 2019 Mar; 17(12):3167-3180. PubMed ID: 30838365
[TBL] [Abstract][Full Text] [Related]
10. Asymmetric induction in methyl ketone aldol additions to alpha-alkoxy and alpha,beta-bisalkoxy aldehydes: a model for acyclic stereocontrol.
Evans DA; Cee VJ; Siska SJ
J Am Chem Soc; 2006 Jul; 128(29):9433-41. PubMed ID: 16848480
[TBL] [Abstract][Full Text] [Related]
11. Understanding the origins of remote asymmetric induction in the boron aldol reactions of beta-alkoxy methyl ketones.
Paton RS; Goodman JM
Org Lett; 2006 Sep; 8(19):4299-302. PubMed ID: 16956211
[TBL] [Abstract][Full Text] [Related]
12. A systematic study of the effects of relative configuration, protecting group, and enolate type on the diastereoselectivities of aldol reactions of a chiral ethyl ketone with 2-methylpropanal.
Ward DE; Kundu D; Biniaz M; Jana S
J Org Chem; 2014 Aug; 79(15):6868-94. PubMed ID: 25029195
[TBL] [Abstract][Full Text] [Related]
13. Temporary silicon connection strategies in intramolecular allylation of aldehydes with allylsilanes.
Beignet J; Jervis PJ; Cox LR
J Org Chem; 2008 Jul; 73(14):5462-75. PubMed ID: 18557649
[TBL] [Abstract][Full Text] [Related]
14. Aldol addition of lithium and boron enolates of 1,3-dioxan-5-ones to aldehydes. A new entry into monosaccharide derivatives.
Majewski M; Nowak P
J Org Chem; 2000 Aug; 65(17):5152-60. PubMed ID: 10993340
[TBL] [Abstract][Full Text] [Related]
15. Transition state models for probing stereoinduction in Evans chiral auxiliary-based asymmetric aldol reactions.
Shinisha CB; Sunoj RB
J Am Chem Soc; 2010 Sep; 132(35):12319-30. PubMed ID: 20707387
[TBL] [Abstract][Full Text] [Related]
16. Lewis base catalyzed aldol additions of chiral trichlorosilyl enolates and silyl enol ethers.
Denmark SE; Fujimori S; Pham SM
J Org Chem; 2005 Dec; 70(26):10823-40. PubMed ID: 16356006
[TBL] [Abstract][Full Text] [Related]
17. Catalytic Use of a Boron Source for Boron Enolate Mediated Stereoselective Aldol Reactions in Water.
Mori Y; Manabe K; Kobayashi S
Angew Chem Int Ed Engl; 2001 Aug; 40(15):2815-2818. PubMed ID: 29712003
[TBL] [Abstract][Full Text] [Related]
18. Asymmetric aldol reaction using boron enolates.
Cergol KM; Coster MJ
Nat Protoc; 2007; 2(10):2568-73. PubMed ID: 17947999
[TBL] [Abstract][Full Text] [Related]
19. Mukaiyama aldol addition to alpha-chloro-substituted aldehydes. Origin of the unexpected syn selectivity.
Borg T; Danielsson J; Somfai P
Chem Commun (Camb); 2010 Feb; 46(8):1281-3. PubMed ID: 20449277
[TBL] [Abstract][Full Text] [Related]
20. Influence of the beta-alkoxy group on the diastereoselectivity of Aldol reactions of tetrahydro-4H-thiopyran-4-one with 4-Alkoxytetrahydro-2H-thiopyran-3-carboxaldehydes.
Ward DE; Sales M; Man CC; Shen J; Sasmal PK; Guo C
J Org Chem; 2002 Mar; 67(5):1618-29. PubMed ID: 11871895
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
