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Items: 1 to 20 of 98

1.

Stereoselective synthesis of multiple stereocenters by using a double aldol reaction.

Shimoda Y, Kubo T, Sugiura M, Kotani S, Nakajima M.

Angew Chem Int Ed Engl. 2013 Mar 18;52(12):3461-4. doi: 10.1002/anie.201209848. Epub 2013 Feb 18. No abstract available.

PMID:
23418113
2.

Lewis base catalysis of the Mukaiyama directed aldol reaction: 40 years of inspiration and advances.

Beutner GL, Denmark SE.

Angew Chem Int Ed Engl. 2013 Aug 26;52(35):9086-96. doi: 10.1002/anie.201302084. Epub 2013 Jul 10. Review.

PMID:
23843275
3.

Enantioselective synthesis of 4-substituted 4,5-dihydro-1H-[1,5]benzodiazepin-2(3H)-ones by the Lewis base-catalyzed hydrosilylation.

Chen X, Zheng Y, Shu C, Yuan W, Liu B, Zhang X.

J Org Chem. 2011 Nov 4;76(21):9109-15. doi: 10.1021/jo201334n. Epub 2011 Oct 7.

PMID:
21958202
4.

Spiro[4,4]-1,6-nonadiene-based diphosphine oxides in lewis base catalyzed asymmetric double-aldol reactions.

Zhang P, Han Z, Wang Z, Ding K.

Angew Chem Int Ed Engl. 2013 Oct 11;52(42):11054-8. doi: 10.1002/anie.201305846. Epub 2013 Aug 27.

PMID:
24038632
5.

Catalytic enantioselective domino oxa-michael/aldol condensations: asymmetric synthesis of benzopyran derivatives.

Sundén H, Ibrahem I, Zhao GL, Eriksson L, Córdova A.

Chemistry. 2007;13(2):574-81.

PMID:
17039558
6.

Diastereo- and enantioselective reductive aldol reaction with trichlorosilane using chiral Lewis bases as organocatalysts.

Sugiura M, Sato N, Sonoda Y, Kotani S, Nakajima M.

Chem Asian J. 2010 Mar 1;5(3):478-81. doi: 10.1002/asia.200900450. No abstract available.

PMID:
20033980
7.

Reductive Hydrazination with Trichlorosilane: A Method for the Preparation of 1,1-Disubstituted Hydrazines.

Wang T, Di X, Wang C, Zhou L, Sun J.

Org Lett. 2016 Apr 15;18(8):1900-3. doi: 10.1021/acs.orglett.6b00675. Epub 2016 Apr 6.

PMID:
27049166
8.

Asymmetric aldol reactions between acetone and benzaldehydes catalyzed by chiral Zn2+ complexes of aminoacyl 1,4,7,10-tetraazacyclododecane: fine-tuning of the amino-acid side chains and a revised reaction mechanism.

Itoh S, Tokunaga T, Sonoike S, Kitamura M, Yamano A, Aoki S.

Chem Asian J. 2013 Sep;8(9):2125-35. doi: 10.1002/asia.201300308. Epub 2013 Jun 18.

PMID:
23780779
9.

Asymmetric catalysis of aldol reactions with chiral lewis bases.

Denmark SE, Stavenger RA.

Acc Chem Res. 2000 Jun;33(6):432-40. Review.

PMID:
10891061
10.

Stereoselective synthesis of aminoindanols via an efficient cascade aza-Michael-aldol reaction.

Qian H, Zhao W, Sung HH, Williams ID, Sun J.

Chem Commun (Camb). 2013 May 14;49(39):4361-3. doi: 10.1039/c2cc37102b. Epub 2012 Nov 21.

PMID:
23169191
11.

Synthesis and chemistry of bridgehead allylsilanes. Stereoselective reactions with aldehydes.

Lauchli R, Whitney JM, Zhu L, Shea KJ.

Org Lett. 2005 Sep 1;7(18):3913-6.

PMID:
16119930
12.

Theoretical studies on the mechanism and stereoselectivity of Rh(Phebox)-catalyzed asymmetric reductive aldol reaction.

Yang YF, Shi T, Zhang XH, Tang ZX, Wen ZY, Quan JM, Wu YD.

Org Biomol Chem. 2011 Aug 21;9(16):5845-55. doi: 10.1039/c1ob05501a. Epub 2011 Jul 8.

PMID:
21743899
13.

Synthesis of aryl group-modified DIOP dioxides (Ar-DIOPOs) and their application as modular Lewis base catalysts.

Ohmaru Y, Sato N, Mizutani M, Kotani S, Sugiura M, Nakajima M.

Org Biomol Chem. 2012 Jun 21;10(23):4562-70. doi: 10.1039/c2ob25338k. Epub 2012 May 9.

PMID:
22569566
14.

Lewis base-catalyzed conjugate reduction and reductive aldol reaction of alpha,beta-unsaturated ketones using trichlorosilane.

Sugiura M, Sato N, Kotani S, Nakajima M.

Chem Commun (Camb). 2008 Sep 28;(36):4309-11. doi: 10.1039/b807529h. Epub 2008 Jul 17.

PMID:
18802553
16.
17.
18.

Dual metal and Lewis base catalysis approach for asymmetric synthesis of dihydroquinolines and the α-arylation of aldehydes via N-acyliminium ions.

Volla CM, Fava E, Atodiresei I, Rueping M.

Chem Commun (Camb). 2015 Nov 11;51(87):15788-91. doi: 10.1039/c5cc05209b.

PMID:
26365533
19.
20.

Regioselective silylation of pyranosides using a boronic acid/Lewis base co-catalyst system.

Lee D, Taylor MS.

Org Biomol Chem. 2013 Sep 7;11(33):5409-12. doi: 10.1039/c3ob40981c.

PMID:
23877384

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