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Items: 1 to 20 of 112

1.

Enantioselective synthesis of all-carbon quaternary stereogenic centers in acyclic systems.

Das JP, Marek I.

Chem Commun (Camb). 2011 Apr 28;47(16):4593-623. doi: 10.1039/c0cc05222a. Epub 2011 Feb 28.

PMID:
21359322
2.

Enantioselective conjugate addition nitro-Mannich reactions: solvent controlled synthesis of acyclic anti- and syn-β-nitroamines with three contiguous stereocenters.

Anderson JC, Stepney GJ, Mills MR, Horsfall LR, Blake AJ, Lewis W.

J Org Chem. 2011 Apr 1;76(7):1961-71. doi: 10.1021/jo102408u. Epub 2011 Feb 1.

PMID:
21284394
3.

Stereoselective construction of quaternary carbon stereocenters via a semipinacol rearrangement strategy.

Wang B, Tu YQ.

Acc Chem Res. 2011 Nov 15;44(11):1207-22. doi: 10.1021/ar200082p. Epub 2011 Jul 6.

PMID:
21728380
6.

All-carbon quaternary stereogenic centers in acyclic systems through the creation of several C-C bonds per chemical step.

Marek I, Minko Y, Pasco M, Mejuch T, Gilboa N, Chechik H, Das JP.

J Am Chem Soc. 2014 Feb 19;136(7):2682-94. doi: 10.1021/ja410424g. Epub 2014 Feb 10.

PMID:
24512113
8.
9.

All-carbon quaternary stereogenic centers by enantioselective cu-catalyzed conjugate additions promoted by a chiral N-heterocyclic carbene.

Brown MK, May TL, Baxter CA, Hoveyda AH.

Angew Chem Int Ed Engl. 2007;46(7):1097-100. No abstract available.

PMID:
17200971
10.
11.

A domino enyne/IMDA approach to the core structure of (-) vinigrol.

Betkekar VV, Sayyad AA, Kaliappan KP.

Org Lett. 2014 Nov 7;16(21):5540-3. doi: 10.1021/ol502497n. Epub 2014 Oct 13.

PMID:
25310274
13.

Enantioselective C-C bond cleavage creating chiral quaternary carbon centers.

Matsuda T, Shigeno M, Makino M, Murakami M.

Org Lett. 2006 Jul 20;8(15):3379-81.

PMID:
16836410
14.

Total synthesis of (-)-teucvidin.

Liu X, Lee CS.

Org Lett. 2012 Jun 1;14(11):2886-9. doi: 10.1021/ol301098s. Epub 2012 May 17.

PMID:
22594711
15.
17.

Stereodefined trisubstituted enolates as a unique entry to all-carbon quaternary stereogenic centers in acyclic systems.

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

Nat Protoc. 2013 Apr;8(4):749-54. doi: 10.1038/nprot.2013.036. Epub 2013 Mar 21.

PMID:
23518666
18.
19.

Enantioselective synthesis of diversely substituted quaternary 1,4-benzodiazepin-2-ones and 1,4-benzodiazepine-2,5-diones.

Carlier PR, Zhao H, MacQuarrie-Hunter SL, DeGuzman JC, Hsu DC.

J Am Chem Soc. 2006 Nov 29;128(47):15215-20.

PMID:
17117873
20.

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

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