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Items: 1 to 20 of 113

1.

Enantioselective and diastereoselective Tsuji-Trost allylic alkylation of lactones: an experimental and computational study.

Meletis P, Patil M, Thiel W, Frank W, Braun M.

Chemistry. 2011 Sep 26;17(40):11243-9. doi: 10.1002/chem.201101406. Epub 2011 Aug 26.

PMID:
21922557
2.

Origin of selectivity of Tsuji-Trost allylic alkylation of lactones: highly ordered transition states with lithium-containing enolates.

Patil M, Thiel W.

Chemistry. 2012 Aug 13;18(33):10408-18. doi: 10.1002/chem.201201267. Epub 2012 Jun 26.

PMID:
22736518
4.

Palladium catalyzed allylic C-H alkylation: a mechanistic perspective.

Engelin CJ, Fristrup P.

Molecules. 2011 Jan 21;16(1):951-69. doi: 10.3390/molecules16010951. Review.

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Deconvoluting the memory effect in Pd-catalyzed allylic alkylation: Effect of leaving group and added chloride.

Fristrup P, Jensen T, Hoppe J, Norrby PO.

Chemistry. 2006 Jul 5;12(20):5352-60.

PMID:
16637086
9.
10.

The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation.

Keith JA, Behenna DC, Sherden N, Mohr JT, Ma S, Marinescu SC, Nielsen RJ, Oxgaard J, Stoltz BM, Goddard WA 3rd.

J Am Chem Soc. 2012 Nov 21;134(46):19050-60. doi: 10.1021/ja306860n. Epub 2012 Nov 6.

11.

TiCl4-promoted Baylis-Hillman reaction: mechanistic rationale toward product distribution and stereoselectivity.

Patel C, Sunoj RB.

J Org Chem. 2010 Jan 15;75(2):359-67. doi: 10.1021/jo902123x.

PMID:
20000733
12.

Intramolecular palladium-catalyzed allylic alkylation: enantio- and diastereoselective synthesis of [2.2.2] bicycles.

Trost BM, Sacchi KL, Schroeder GM, Asakawa N.

Org Lett. 2002 Oct 3;4(20):3427-30.

PMID:
12323035
13.

Transition state models for probing stereoinduction in Evans chiral auxiliary-based asymmetric aldol reactions.

Shinisha CB, Sunoj RB.

J Am Chem Soc. 2010 Sep 8;132(35):12319-30. doi: 10.1021/ja101913k.

PMID:
20707387
14.

Counterintuitive kinetics in Tsuji-Trost allylation: ion-pair partitioning and implications for asymmetric catalysis.

Evans LA, Fey N, Harvey JN, Hose D, Lloyd-Jones GC, Murray P, Orpen AG, Osborne R, Owen-Smith GJ, Purdie M.

J Am Chem Soc. 2008 Nov 5;130(44):14471-3. doi: 10.1021/ja806278e. Epub 2008 Oct 8.

PMID:
18839958
15.

On the origin of the stereoselectivity in the alkylation of oxazolopiperidone enolates.

Soteras I, Lozano O, Gómez-Esqué A, Escolano C, Orozco M, Amat M, Bosch J, Luque FJ.

J Am Chem Soc. 2006 May 24;128(20):6581-8.

PMID:
16704257
17.

Beta-amino alcohol derived beta-hydroxy- and beta-(o-diphenylphosphino)benzoyloxy(o-diphenylphosphino)benzamides: an ester-amide ligand structural model for the palladium-catalyzed allylic alkylation reaction.

Mahadik GS, Knott SA, Szczepura LF, Peters SJ, Standard JM, Hitchcock SR.

J Org Chem. 2009 Nov 6;74(21):8164-73. doi: 10.1021/jo9016474.

PMID:
19807143
18.

Alkali metals (Li, Na, and K) in methyl phosphodiester hydrolysis.

Pinjari RV, Kaptan SS, Gejji SP.

Phys Chem Chem Phys. 2009 Jul 14;11(26):5253-62. doi: 10.1039/b812000e. Epub 2009 Apr 16.

PMID:
19551192
20.

Michael reactions of pseudoephedrine amide enolates: effect of LiCl on syn/anti selectivity.

Smitrovich JH, DiMichele L, Qu C, Boice GN, Nelson TD, Huffman MA, Murry J.

J Org Chem. 2004 Mar 19;69(6):1903-8.

PMID:
15058935
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