Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 104

1.

Chemoselective Catalytic Asymmetric Synthesis of Functionalized Aminals Through the Umpolung Organocascade Reaction of α-Imino Amides.

Yoshida Y, Omori K, Hiroshige T, Mino T, Sakamoto M.

Chem Asian J. 2019 Aug 1;14(15):2737-2743. doi: 10.1002/asia.201900764. Epub 2019 Jul 8.

PMID:
31190370
2.

Chemo- and Regioselective Asymmetric Synthesis of Cyclic Enamides through the Catalytic Umpolung Organocascade Reaction of α-Imino Amides.

Yoshida Y, Hiroshige T, Omori K, Mino T, Sakamoto M.

J Org Chem. 2019 Jun 7;84(11):7362-7371. doi: 10.1021/acs.joc.9b01036. Epub 2019 May 23.

PMID:
31074984
3.

Organocatalytic Highly Regio- and Enantioselective Umpolung Michael Addition Reaction of α-Imino Esters.

Yoshida Y, Mino T, Sakamoto M.

Chemistry. 2017 Sep 18;23(52):12749-12753. doi: 10.1002/chem.201703479. Epub 2017 Aug 29.

PMID:
28796398
6.

Asymmetric synthesis of drug-like spiro[chroman-3,3'-indolin]-2'-ones through aminal-catalysis.

Ramachary DB, Prasad MS, Laxmi SV, Madhavachary R.

Org Biomol Chem. 2014 Jan 28;12(4):574-80. doi: 10.1039/c3ob42100g.

PMID:
24297104
7.

Managing highly coordinative substrates in asymmetric catalysis: a catalytic asymmetric amination with a lanthanum-based ternary catalyst.

Mashiko T, Kumagai N, Shibasaki M.

J Am Chem Soc. 2009 Oct 21;131(41):14990-9. doi: 10.1021/ja9052653.

PMID:
19785408
8.

Catalytic, enantioselective alkylation of alpha-imino esters: the synthesis of nonnatural alpha-amino acid derivatives.

Ferraris D, Young B, Cox C, Dudding T, Drury WJ 3rd, Ryzhkov L, Taggi AE, Lectka T.

J Am Chem Soc. 2002 Jan 9;124(1):67-77.

PMID:
11772063
9.

Catalytic Asymmetric Synthesis of Chiral γ-Amino Ketones via Umpolung Reactions of Imines.

Hu L, Wu Y, Li Z, Deng L.

J Am Chem Soc. 2016 Dec 14;138(49):15817-15820. Epub 2016 Nov 30. Erratum in: J Am Chem Soc. 2017 Jan 11;139(1):562.

10.
11.

Direct asymmetric reductive amination.

Steinhuebel D, Sun Y, Matsumura K, Sayo N, Saito T.

J Am Chem Soc. 2009 Aug 19;131(32):11316-7. doi: 10.1021/ja905143m.

PMID:
19637921
12.

De novo synthesis of Tamiflu via a catalytic asymmetric ring-opening of meso-aziridines with TMSN3.

Fukuta Y, Mita T, Fukuda N, Kanai M, Shibasaki M.

J Am Chem Soc. 2006 May 17;128(19):6312-3.

PMID:
16683784
13.

Catalytic asymmetric synthesis of R207910.

Saga Y, Motoki R, Makino S, Shimizu Y, Kanai M, Shibasaki M.

J Am Chem Soc. 2010 Jun 16;132(23):7905-7. doi: 10.1021/ja103183r.

PMID:
20481617
14.

Asymmetric Aminalization via Cation-Binding Catalysis.

Park SY, Liu Y, Oh JS, Kweon YK, Jeong YB, Duan M, Tan Y, Lee JW, Yan H, Song CE.

Chemistry. 2018 Jan 24;24(5):1020-1025. doi: 10.1002/chem.201703800. Epub 2017 Dec 5.

PMID:
28833708
16.

Asymmetric Catalytic Aza-Diels-Alder/Ring-Closing Cascade Reaction Forming Bicyclic Azaheterocycles by Trienamine Catalysis.

Li Y, Barløse C, Jørgensen J, Carlsen BD, Jørgensen KA.

Chemistry. 2017 Jan 1;23(1):38-41. doi: 10.1002/chem.201604310. Epub 2016 Nov 9.

PMID:
27779801
17.

Umpolung Reactions of α-Imino Esters: Useful Methods for the Preparation of α-Amino Acid Frameworks.

Mizota I, Shimizu M.

Chem Rec. 2016 Apr;16(2):688-702. doi: 10.1002/tcr.201500267. Epub 2016 Feb 2.

PMID:
26833635
18.

Catalytic Asymmetric Umpolung Allylation/2-Aza-Cope Rearrangement for the Construction of α-Tetrasubstituted α-Trifluoromethyl Homoallylic Amines.

Shen C, Wang RQ, Wei L, Wang ZF, Tao HY, Wang CJ.

Org Lett. 2019 Aug 19. doi: 10.1021/acs.orglett.9b02543. [Epub ahead of print]

PMID:
31424222
19.

One-Pot Three-Component Synthesis of Vicinal Diamines via In Situ Aminal Formation and Carboamination.

Orcel U, Waser J.

Angew Chem Int Ed Engl. 2016 Oct 4;55(41):12881-5. doi: 10.1002/anie.201607318. Epub 2016 Sep 16.

PMID:
27633551
20.

A designed amide as an aldol donor in the direct catalytic asymmetric aldol reaction.

Weidner K, Kumagai N, Shibasaki M.

Angew Chem Int Ed Engl. 2014 Jun 10;53(24):6150-4. doi: 10.1002/anie.201403118. Epub 2014 Apr 30.

PMID:
24789121

Supplemental Content

Support Center