171 related articles for article (PubMed ID: 15548041)
1. CamTHP*OH: a camphor-derived delta-lactol auxiliary for the effective desymmetrization of attached glycinamide residues. Asymmetric synthesis of alpha-amino carbonyl compounds.
Dixon DJ; Horan RA; Monck NJ
Org Lett; 2004 Nov; 6(24):4423-6. PubMed ID: 15548041
[TBL] [Abstract][Full Text] [Related]
2. Highly stereoselective Michael addition reactions of CamTHP*-desymmetrized glycinamide for the synthesis of functionally dense amino acid derivatives.
Dixon DJ; Horan RA; Monck NJ; Berg P
Org Lett; 2004 Nov; 6(24):4427-9. PubMed ID: 15548042
[TBL] [Abstract][Full Text] [Related]
3. Highly enantioselective phase-transfer-catalyzed alkylation of protected alpha-amino acid amides toward practical asymmetric synthesis of vicinal diamines, alpha-amino ketones, and alpha-amino alcohols.
Ooi T; Takeuchi M; Kato D; Uematsu Y; Tayama E; Sakai D; Maruoka K
J Am Chem Soc; 2005 Apr; 127(14):5073-83. PubMed ID: 15810842
[TBL] [Abstract][Full Text] [Related]
4. Highly stereoselective intermolecular oxy-michael addition reaction to alpha,beta-unsaturated malonate esters.
Buchanan DJ; Dixon DJ; Hernandez-Juan FA
Org Lett; 2004 Apr; 6(9):1357-60. PubMed ID: 15101741
[TBL] [Abstract][Full Text] [Related]
5. Asymmetric synthesis of alpha-amino 1,3-dithioketals from sulfinimines (N-sulfinyl imines). Synthesis of (2S,3R)-(-)-3-hydroxy-3-methylproline.
Davis FA; Ramachandar T; Liu H
Org Lett; 2004 Sep; 6(19):3393-5. PubMed ID: 15355060
[TBL] [Abstract][Full Text] [Related]
6. Highly stereoselective oxy-michael additions to beta,gamma-unsaturated alpha-keto esters: rapid enantioselective synthesis of 3-hydroxybutenolides.
Xiong X; Ovens C; Pilling AW; Ward JW; Dixon DJ
Org Lett; 2008 Feb; 10(4):565-7. PubMed ID: 18211073
[TBL] [Abstract][Full Text] [Related]
7. Diastereoselective addition of chlorotitanium enolate of N-acyl thiazolidinethione to O-methyl oximes: a novel, stereoselective synthesis of alpha,beta-disubstituted beta-amino carbonyl compounds via chiral auxiliary mediated azetine formation.
Ambhaikar NB; Snyder JP; Liotta DC
J Am Chem Soc; 2003 Apr; 125(13):3690-1. PubMed ID: 12656586
[TBL] [Abstract][Full Text] [Related]
8. Bridgehead enolates: substitution and asymmetric desymmetrization of small bridged carbonyl compounds by lithium amide bases.
Giblin GM; Kirk DT; Mitchell L; Simpkins NS
Org Lett; 2003 May; 5(10):1673-5. PubMed ID: 12735749
[TBL] [Abstract][Full Text] [Related]
9. Tandem asymmetric conjugate addition/alpha-alkylation using (S,S)-(+)-pseudoephedrine as chiral auxiliary.
Reyes E; Vicario JL; Carrillo L; Badía D; Iza A; Uria U
Org Lett; 2006 Jun; 8(12):2535-8. PubMed ID: 16737307
[TBL] [Abstract][Full Text] [Related]
10. The domino multicomponent allylation reaction for the stereoselective synthesis of homoallylic alcohols.
Tietze LF; Kinzel T; Brazel CC
Acc Chem Res; 2009 Feb; 42(2):367-78. PubMed ID: 19154154
[TBL] [Abstract][Full Text] [Related]
11. Asymmetric synthesis of beta-amino carbonyl compounds with N-sulfinyl beta-amino Weinreb amides.
Davis FA; Nolt MB; Wu Y; Prasad KR; Li D; Yang B; Bowen K; Lee SH; Eardley JH
J Org Chem; 2005 Mar; 70(6):2184-90. PubMed ID: 15760203
[TBL] [Abstract][Full Text] [Related]
12. Direct amino acid-catalyzed asymmetric desymmetrization of meso-compounds: tandem aminoxylation/O-N bond heterolysis reactions.
Ramachary DB; Barbas CF
Org Lett; 2005 Apr; 7(8):1577-80. PubMed ID: 15816756
[TBL] [Abstract][Full Text] [Related]
13. Asymmetric synthesis of alpha,alpha-disubstituted alpha-amino acids by diastereoselective alkylation of camphor-based tricyclic iminolactone.
Xu PF; Li S; Lu TJ; Wu CC; Fan B; Golfis G
J Org Chem; 2006 Jun; 71(12):4364-73. PubMed ID: 16749763
[TBL] [Abstract][Full Text] [Related]
14. Asymmetric synthesis of the highly potent anti-metastatic prostacyclin analogue cicaprost and its isomer isocicaprost.
Lerm M; Gais HJ; Cheng K; Vermeeren C
J Am Chem Soc; 2003 Aug; 125(32):9653-67. PubMed ID: 12904032
[TBL] [Abstract][Full Text] [Related]
15. N-sulfinyl beta-amino Weinreb amides: synthesis of enantiopure beta-amino carbonyl compounds. Asymmetric synthesis of (+)-sedridine and (-)-allosedridine.
Davis FA; Prasad KR; Nolt MB; Wu Y
Org Lett; 2003 Mar; 5(6):925-7. PubMed ID: 12633107
[TBL] [Abstract][Full Text] [Related]
16. Highly diastereoselective Michael addition reactions of butane-2,3-diacetal desymmetrized glycolic acid. Preparation of alpha-hydroxy-gamma-amino acid derivatives.
Dixon DJ; Ley SV; Rodríguez F
Org Lett; 2001 Nov; 3(23):3753-5. PubMed ID: 11700130
[TBL] [Abstract][Full Text] [Related]
17. Chiral oxime ethers in asymmetric synthesis. O-(1-Phenylbutyl)benzyloxyacetaldoxime, a versatile reagent for the asymmetric synthesis of protected 1,2-aminoalcohols, alpha-amino acid derivatives, and 2-hydroxymethyl nitrogen heterocycles including iminosugars.
Cooper TS; Larigo AS; Laurent P; Moody CJ; Takle AK
Org Biomol Chem; 2005 Apr; 3(7):1252-62. PubMed ID: 15785815
[TBL] [Abstract][Full Text] [Related]
18. (S,S)-(+)-pseudoephedrine alpha-iminoglyoxylamide as a chiral glycine cation equivalent: a modular and flexible approach to enantioenriched alpha-amino ketones.
Ruiz N; Vicario JL; Badía D; Carrillo L; Alonso B
Org Lett; 2008 Jun; 10(12):2613-6. PubMed ID: 18489102
[TBL] [Abstract][Full Text] [Related]
19. An advance on exploring N-tert-butanesulfinyl imines in asymmetric synthesis of chiral amines.
Lin GQ; Xu MH; Zhong YW; Sun XW
Acc Chem Res; 2008 Jul; 41(7):831-40. PubMed ID: 18533688
[TBL] [Abstract][Full Text] [Related]
20. Highly diastereoselective lithium enolate aldol reactions of butane-2,3-diacetal desymmetrized glycolic acid and deprotection to enantiopure anti-2,3-dihydroxy esters.
Dixon DJ; Ley SV; Polara A; Sheppard T
Org Lett; 2001 Nov; 3(23):3749-52. PubMed ID: 11700129
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
