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Items: 1 to 20 of 114

1.

Convergent diastereoselective preparation of adjacent quaternary stereocenters in an acyclic system.

Mejuch T, Dutta B, Botoshansky M, Marek I.

Org Biomol Chem. 2012 Aug 14;10(30):5803-6. doi: 10.1039/c2ob25121c. Epub 2012 Mar 8.

PMID:
22402794
2.

Combined carbometalation-zinc homologation-allylation reactions as a new approach for alkoxyallylation of aldehydes.

Mejuch T, Botoshansky M, Marek I.

Org Lett. 2011 Jul 15;13(14):3604-7. doi: 10.1021/ol201221d. Epub 2011 Jun 15.

PMID:
21675728
3.

Forming Stereogenic Centers in Acyclic Systems from Alkynes.

Vabre R, Island B, Diehl CJ, Schreiner PR, Marek I.

Angew Chem Int Ed Engl. 2015 Aug 17;54(34):9996-9. doi: 10.1002/anie.201504756. Epub 2015 Jun 30.

PMID:
26130570
4.

Axial preferences in allylation reactions via the Zimmerman-Traxler transition state.

Mejuch T, Gilboa N, Gayon E, Wang H, Houk KN, Marek I.

Acc Chem Res. 2013 Jul 16;46(7):1659-69. doi: 10.1021/ar4000532. Epub 2013 May 14. Review.

5.
6.

Highly diastereoselective construction of acyclic systems with two adjacent quaternary stereocenters by allylation of ketones.

Takeda T, Yamamoto M, Yoshida S, Tsubouchi A.

Angew Chem Int Ed Engl. 2012 Jul 16;51(29):7263-6. doi: 10.1002/anie.201202808. Epub 2012 Jun 8.

PMID:
22684935
8.

Stereoselective Formation of Fully Substituted Ketone Enolates.

Haimov E, Nairoukh Z, Shterenberg A, Berkovitz T, Jamison TF, Marek I.

Angew Chem Int Ed Engl. 2016 Apr 25;55(18):5517-20. doi: 10.1002/anie.201601883. Epub 2016 Mar 29.

PMID:
27027778
9.

Enantioselective allylic alkylation of stereodefined polysubstituted copper enolates as an entry to acyclic quaternary carbon stereocentres.

Nairoukh Z, Kumar GGKSN, Minko Y, Marek I.

Chem Sci. 2017 Jan 1;8(1):627-630. doi: 10.1039/c6sc03036j. Epub 2016 Sep 15.

10.

Forming all-carbon quaternary stereogenic centres in acyclic systems from alkynes.

Minko Y, Pasco M, Lercher L, Botoshansky M, Marek I.

Nature. 2012 Oct 25;490(7421):522-6. doi: 10.1038/nature11569.

PMID:
23099407
11.
13.

Four-component reactions for a new diastereoselective synthesis of chiral quaternary centers.

Sklute G, Amsallem D, Shabli A, Varghese JP, Marek I.

J Am Chem Soc. 2003 Oct 1;125(39):11776-7.

PMID:
14505373
14.

Stereodefined Acyclic Polysubstituted Silyl Ketene Aminals: Asymmetric Formation of Aldol Products with Quaternary Carbon Stereocenters.

Nairoukh Z, Marek I.

Angew Chem Int Ed Engl. 2015 Nov 23;54(48):14393-7. doi: 10.1002/anie.201507209. Epub 2015 Oct 8.

PMID:
26448575
15.

Highly diastereoselective and enantiospecific allylation of ketones and imines using borinic esters: contiguous quaternary stereogenic centers.

Chen JL, Aggarwal VK.

Angew Chem Int Ed Engl. 2014 Oct 6;53(41):10992-6. doi: 10.1002/anie.201407127. Epub 2014 Aug 25.

PMID:
25156948
16.

Highly diastereoselective synthesis of vicinal quaternary and tertiary stereocenters using the iodo-aldol cyclization.

Douelle F, Capes AS, Greaney MF.

Org Lett. 2007 May 10;9(10):1931-4. Epub 2007 Apr 11.

PMID:
17425327
17.

Diastereoselective osmium-catalyzed vicinal oxyamination of acyclic allylic alcohol derivatives.

Masruri, Kanizaj N, McLeod MD.

Chirality. 2014 Nov;26(11):724-33.

PMID:
25513679
18.

Highly enantio- and diastereoselective one-pot synthesis of acyclic epoxy alcohols and allylic epoxy alcohols.

Kelly AR, Lurain AE, Walsh PJ.

J Am Chem Soc. 2005 Oct 26;127(42):14668-74.

PMID:
16231920
19.

Modulable and highly diastereoselective carbometalations of cyclopropenes.

Didier D, Delaye PO, Simaan M, Island B, Eppe G, Eijsberg H, Kleiner A, Knochel P, Marek I.

Chemistry. 2014 Jan 20;20(4):1038-48. doi: 10.1002/chem.201303569. Epub 2013 Dec 12.

PMID:
24338953

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