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Items: 1 to 20 of 2278

  • The following term was not found in PubMed: 12037-12047.
1.

Mechanisms of hydride abstractions by quinones.

Guo X, Zipse H, Mayr H.

J Am Chem Soc. 2014 Oct 1;136(39):13863-73. doi: 10.1021/ja507598y. Epub 2014 Sep 19.

PMID:
25196576
2.

Quantification of the ambident electrophilicities of halogen-substituted quinones.

Guo X, Mayr H.

J Am Chem Soc. 2014 Aug 13;136(32):11499-512. doi: 10.1021/ja505613b. Epub 2014 Aug 5.

PMID:
25053179
3.

Nucleophilicity parameters of pyridinium ylides and their use in mechanistic analyses.

Allgäuer DS, Mayer P, Mayr H.

J Am Chem Soc. 2013 Oct 9;135(40):15216-24. doi: 10.1021/ja407885h. Epub 2013 Sep 25.

PMID:
24020381
4.

Electrophilicities of benzaldehyde-derived iminium ions: quantification of the electrophilic activation of aldehydes by iminium formation.

Appel R, Chelli S, Tokuyasu T, Troshin K, Mayr H.

J Am Chem Soc. 2013 May 1;135(17):6579-87. doi: 10.1021/ja401106x. Epub 2013 Apr 23.

PMID:
23570344
5.

Exploring the electron transfer pathways in photosystem I by high-time-resolution electron paramagnetic resonance: observation of the B-side radical pair P700(+)A1B(-) in whole cells of the deuterated green alga Chlamydomonas reinhardtii at cryogenic temperatures.

Berthold T, von Gromoff ED, Santabarbara S, Stehle P, Link G, Poluektov OG, Heathcote P, Beck CF, Thurnauer MC, Kothe G.

J Am Chem Soc. 2012 Mar 28;134(12):5563-76. doi: 10.1021/ja208806g. Epub 2012 Mar 16.

PMID:
22352450
6.

Quantification of the electrophilic reactivities of aldehydes, imines, and enones.

Appel R, Mayr H.

J Am Chem Soc. 2011 Jun 1;133(21):8240-51. doi: 10.1021/ja200820m. Epub 2011 May 5.

PMID:
21553901
7.

Can one predict changes from S(N)1 to S(N)2 mechanisms?

Phan TB, Nolte C, Kobayashi S, Ofial AR, Mayr H.

J Am Chem Soc. 2009 Aug 19;131(32):11392-401. doi: 10.1021/ja903207b.

PMID:
19634906
8.
9.

Involvement of water in carbohydrate-protein binding: concanavalin A revisited.

Kadirvelraj R, Foley BL, Dyekjaer JD, Woods RJ.

J Am Chem Soc. 2008 Dec 17;130(50):16933-42. doi: 10.1021/ja8039663.

10.

Are the radical centers in peptide radical cations mobile? The generation, tautomerism, and dissociation of isomeric alpha-carbon-centered triglycine radical cations in the gas phase.

Chu IK, Zhao J, Xu M, Siu SO, Hopkinson AC, Siu KW.

J Am Chem Soc. 2008 Jun 25;130(25):7862-72. doi: 10.1021/ja801108j. Epub 2008 May 31.

PMID:
18512915
11.
12.

Spectroscopic identification of different types of copper centers generated in synthetic four-helix bundle proteins.

Schnepf R, Haehnel W, Wieghardt K, Hildebrandt P.

J Am Chem Soc. 2004 Nov 10;126(44):14389-99.

PMID:
15521758
13.
14.
15.

Designing libraries of first generation AB3 and AB2 self-assembling dendrons via the primary structure generated from combinations of (AB)(y)-AB3 and (AB)(y)-AB2 building blocks.

Percec V, Mitchell CM, Cho WD, Uchida S, Glodde M, Ungar G, Zeng X, Liu Y, Balagurusamy VS, Heiney PA.

J Am Chem Soc. 2004 May 19;126(19):6078-94.

PMID:
15137774
16.

A novel RNA motif based on the structure of unusually stable 2',5'-linked r(UUCG) loops.

Denisov AY, Hannoush RN, Gehring K, Damha MJ.

J Am Chem Soc. 2003 Sep 24;125(38):11525-31.

PMID:
13129354
17.

NMR studies of DNA single strands and DNA:RNA hybrids with and without 1-propynylation at C5 of oligopyrimidines.

Znosko BM, Barnes TW 3rd, Krugh TR, Turner DH.

J Am Chem Soc. 2003 May 21;125(20):6090-7.

PMID:
12785839
18.

NMR determination of the conformation of a trimethylene interstrand cross-link in an oligodeoxynucleotide duplex containing a 5'-d(GpC) motif.

Dooley PA, Zhang M, Korbel GA, Nechev LV, Harris CM, Stone MP, Harris TM.

J Am Chem Soc. 2003 Jan 8;125(1):62-72.

PMID:
12515507
19.

Orbital symmetry as a tool for understanding the bonding in Krossing's cation.

Deubel DV.

J Am Chem Soc. 2002 Oct 16;124(41):12312-8.

PMID:
12371875
20.

Phospholipid bicelles that align with their normals parallel to the magnetic field.

Tan C, Fung BM, Cho G.

J Am Chem Soc. 2002 Oct 2;124(39):11827-32.

PMID:
12296750

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