+++@cc. Chem. Res.

[Chem_DM]

Нескромный запрос.
1. Acc. Chem. Res.,
Dynamic Monte Carlo Simulations of Surface-Rate Processes
H. Kang, W. Weinberg
1992, 25 (6), pp 253–259

Код: Выделить всё

http://dx.doi.org/10.1021/ar00018a600

2. Acc. Chem. Res.,
Strategy of research on supported metal catalysts. Problems of structure-sensitive reactions in the gas phase
Geoffrey C. Bond
1993, 26 (9), pp 490–495

Код: Выделить всё

http://dx.doi.org/10.1021/ar00033a006

3. Acc. Chem. Res.,
Patterned Self-Assembled Monolayers and Meso-Scale Phenomena
Amit Kumar, Nicholas L. Abbott, Hans A. Biebuyck, Enoch Kim, George M. Whitesides
1995, 28 (5), pp 219–226

Код: Выделить всё

http://dx.doi.org/10.1021/ar00053a003

4. Acc. Chem. Res.,
Dissolved Alkali Metals in Zeolites
Peter P. Edwards* and Paul A. Anderson
1996, 29 (1), pp 23–29

Код: Выделить всё

http://dx.doi.org/10.1021/ar950152c

5. Acc. Chem. Res.,
Entropically Driven Order in Crowded Solutions: From Liquid Crystals to Cell Biology
Judith Herzfeld
1996, 29 (1), pp 31–37

Код: Выделить всё

http://dx.doi.org/10.1021/ar9500224

6. Acc. Chem. Res.,
Gallanes, Gallenes, Cyclogallenes, and Gallynes: Organometallic Chemistry about the Gallium?Gallium Bond
Gregory H. Robinson
1999, 32 (9), pp 773–782

Код: Выделить всё

http://dx.doi.org/10.1021/ar980135y

7. Acc. Chem. Res.,
Transient Species in the Stepwise Interconversion of NADH and NAD+
Jerzy Gbicki,* Andrzej Marcinek,* and Jacek Zielonka
2004, 37 (6), pp 379–386

Код: Выделить всё

http://dx.doi.org/10.1021/ar030171j

8. Acc. Chem. Res.,
Knowledge of the Proposed Chemical Mechanism of Action and Cytochrome P450 Metabolism of Antimalarial Trioxanes Like Artemisinin Allows Rational Design of New Antimalarial Peroxides
Gary H. Posner*† and Paul M. O'Neill‡
2004, 37 (6), pp 397–404

Код: Выделить всё

http://dx.doi.org/10.1021/ar020227u

9. Acc. Chem. Res.,
Reactions of the Diiron Enzyme Stearoyl-Acyl Carrier Protein Desaturase
Brian G. Fox,* Karen S. Lyle, and Corina E. Rogge
2004, 37 (7), pp 421–429

Код: Выделить всё

http://dx.doi.org/10.1021/ar030186h

10. Acc. Chem. Res.,
Role of Glycosaminoglycans in Cellular Communication
Robert J. Linhardt*† and Toshihiko Toida‡
2004, 37 (7), pp 431–438

Код: Выделить всё

http://dx.doi.org/10.1021/ar030138x

11. Acc. Chem. Res.,
Ketone-Catalyzed Asymmetric Epoxidation Reactions
Dan Yang*
2004, 37 (8), pp 497–505

Код: Выделить всё

http://dx.doi.org/10.1021/ar030065h

12. Acc. Chem. Res.,
The Enantioselective Synthesis of ?-Amino Acids by Phase-Transfer Catalysis with Achiral Schiff Base Esters
Martin J. O'Donnell
2004, 37 (8), pp 506–517

Код: Выделить всё

http://dx.doi.org/10.1021/ar0300625

13. Acc. Chem. Res.,
Asymmetric Organocatalysis of Structurally Well-Defined Chiral Quaternary Ammonium Fluorides
Takashi Ooi and Keiji Maruoka*
2004, 37 (8), pp 526–533

Код: Выделить всё

http://dx.doi.org/10.1021/ar030060k

14. Acc. Chem. Res.,
Nucleophilic Carbenes in Asymmetric Organocatalysis
Dieter Enders* and Tim Balensiefer
2004, 37 (8), pp 534–541

Код: Выделить всё

http://dx.doi.org/10.1021/ar030050j

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Кроме 4 и 5 - pdf не дает

[Chem_DM]

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