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Results: 1 to 20 of 132

1.

Aminocatalytic asymmetric exo-Diels-Alder reaction with methiodide salts of Mannich bases and 2,4-dienals to construct chiral spirocycles.

Zhang SJ, Zhang J, Zhou QQ, Dong L, Chen YC.

Org Lett. 2013 Feb 15;15(4):968-71. doi: 10.1021/ol4002015. Epub 2013 Feb 7.

PMID:
23391251
[PubMed - indexed for MEDLINE]
2.

Aminocatalytic asymmetric Diels-Alder reactions via HOMO activation.

Li JL, Liu TY, Chen YC.

Acc Chem Res. 2012 Sep 18;45(9):1491-500. doi: 10.1021/ar3000822. Epub 2012 Jun 20.

PMID:
22716926
[PubMed - indexed for MEDLINE]
3.

Aminocatalyzed asymmetric Diels-Alder reaction of 2,4-dienals and rhodanine/hydantoin derivatives.

Zhu K, Huang H, Wu W, Wei Y, Ye J.

Chem Commun (Camb). 2013 Mar 14;49(21):2157-9. doi: 10.1039/c3cc00023k. Epub 2013 Feb 7.

PMID:
23389754
[PubMed - indexed for MEDLINE]
4.

anti-selective direct asymmetric Mannich reactions catalyzed by axially chiral amino sulfonamide as an organocatalyst.

Kano T, Yamaguchi Y, Tokuda O, Maruoka K.

J Am Chem Soc. 2005 Nov 30;127(47):16408-9.

PMID:
16305223
[PubMed - indexed for MEDLINE]
5.

exo-Selective asymmetric Diels-Alder reaction of 2,4-dienals and nitroalkenes by trienamine catalysis.

Jia ZJ, Zhou Q, Zhou QQ, Chen PQ, Chen YC.

Angew Chem Int Ed Engl. 2011 Sep 5;50(37):8638-41. doi: 10.1002/anie.201102013. Epub 2011 Jul 22. No abstract available.

PMID:
21786371
[PubMed - indexed for MEDLINE]
6.

An asymmetric Diels-Alder reaction catalyzed by chiral phosphate magnesium complexes: highly enantioselective synthesis of chiral spirooxindoles.

Li G, Liang T, Wojtas L, Antilla JC.

Angew Chem Int Ed Engl. 2013 Apr 22;52(17):4628-32. doi: 10.1002/anie.201209295. Epub 2013 Mar 20.

PMID:
23519960
[PubMed - indexed for MEDLINE]
7.

Catalytic asymmetric synthesis of spirooxindoles by a mannich-type reaction of isothiocyanato oxindoles.

Kato S, Yoshino T, Shibasaki M, Kanai M, Matsunaga S.

Angew Chem Int Ed Engl. 2012 Jul 9;51(28):7007-10. doi: 10.1002/anie.201203005. Epub 2012 Jun 4.

PMID:
22674857
[PubMed - indexed for MEDLINE]
8.

The direct organocatalytic asymmetric mannich reaction: unmodified aldehydes as nucleophiles.

Notz W, Tanaka F, Watanabe S, Chowdari NS, Turner JM, Thayumanavan R, Barbas CF 3rd.

J Org Chem. 2003 Dec 12;68(25):9624-34.

PMID:
14656087
[PubMed - indexed for MEDLINE]
9.

1-Azadienes as regio- and chemoselective dienophiles in aminocatalytic asymmetric Diels-Alder reaction.

Ma C, Gu J, Teng B, Zhou QQ, Li R, Chen YC.

Org Lett. 2013 Dec 20;15(24):6206-9. doi: 10.1021/ol4030474. Epub 2013 Nov 11.

PMID:
24215629
[PubMed - indexed for MEDLINE]
10.

An achiral-acid-induced switch in the enantioselectivity of a chiral cis-diamine-based organocatalyst for asymmetric aldol and Mannich reactions.

Moteki SA, Han J, Arimitsu S, Akakura M, Nakayama K, Maruoka K.

Angew Chem Int Ed Engl. 2012 Jan 27;51(5):1187-90. doi: 10.1002/anie.201107239. Epub 2011 Dec 21. No abstract available.

PMID:
22190385
[PubMed - indexed for MEDLINE]
11.

The proline-catalyzed direct asymmetric three-component Mannich reaction: scope, optimization, and application to the highly enantioselective synthesis of 1,2-amino alcohols.

List B, Pojarliev P, Biller WT, Martin HJ.

J Am Chem Soc. 2002 Feb 6;124(5):827-33.

PMID:
11817958
[PubMed - indexed for MEDLINE]
12.

An asymmetric normal-electron-demand aza-Diels-Alder reaction via trienamine catalysis.

Liu JX, Zhou QQ, Deng JG, Chen YC.

Org Biomol Chem. 2013 Dec 21;11(47):8175-8. doi: 10.1039/c3ob41698d. Epub 2013 Nov 6.

PMID:
24193264
[PubMed - indexed for MEDLINE]
13.

Antimony(III) chloride catalyzed direct three component one-pot Mannich reaction.

Shukla P, Chattopadhyay N, Nayak SK.

Nat Prod Commun. 2009 Feb;4(2):247-50.

PMID:
19370932
[PubMed - indexed for MEDLINE]
14.

Asymmetric dearomatic Diels-Alder reactions of diverse heteroarenes via π-system activation.

Xiao YC, Yue CZ, Chen PQ, Chen YC.

Org Lett. 2014 Jun 20;16(12):3208-11. doi: 10.1021/ol501217u. Epub 2014 Jun 3.

PMID:
24892780
[PubMed - indexed for MEDLINE]
15.

Asymmetric quadruple aminocatalytic domino reactions to fused carbocycles incorporating a spirooxindole motif.

Jiang K, Jia ZJ, Yin X, Wu L, Chen YC.

Org Lett. 2010 Jun 18;12(12):2766-9. doi: 10.1021/ol100857s.

PMID:
20481511
[PubMed - indexed for MEDLINE]
16.

Asymmetric Diels-Alder reaction of 2-methyl-3-indolylmethanols via in situ generation of o-quinodimethanes.

Xiao YC, Zhou QQ, Dong L, Liu TY, Chen YC.

Org Lett. 2012 Dec 7;14(23):5940-3. doi: 10.1021/ol302853m. Epub 2012 Nov 27.

PMID:
23186032
[PubMed - indexed for MEDLINE]
17.
18.

Amine-N-heterocyclic carbene cascade catalysis for the asymmetric synthesis of fused indane derivatives with multiple chiral centres.

Jia ZJ, Jiang K, Zhou QQ, Dong L, Chen YC.

Chem Commun (Camb). 2013 Jul 4;49(52):5892-4. doi: 10.1039/c3cc42823k. Epub 2013 May 28.

PMID:
23712483
[PubMed - indexed for MEDLINE]
19.

Demonstration of spontaneous chiral symmetry breaking in asymmetric Mannich and Aldol reactions.

Mauksch M, Tsogoeva SB, Wei S, Martynova IM.

Chirality. 2007 Nov;19(10):816-25.

PMID:
17786910
[PubMed - indexed for MEDLINE]
20.

A mild and efficient one-pot synthesis of β-amino carbonyl compounds via Mannich reaction under ambient temperature condition.

Goswami SV, Thorat PB, Chakrawar AV, Bhusare SR.

Mol Divers. 2013 Feb;17(1):33-40. doi: 10.1007/s11030-012-9414-x. Epub 2013 Jan 4.

PMID:
23288546
[PubMed - indexed for MEDLINE]

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