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[iga22]

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1. Pd-Catalyzed Ortho-C-H Acylation/Cross Coupling of Aryl Ketone O-Methyl Oximes with Aldehydes Using tert-Butyl Hydroperoxide as Oxidant
Chun-Wo Chan, Zhongyuan Zhou, Albert S. C. Chan and Wing-Yiu Yu
Org. Lett., Article ASAP

DOI:

http://dx.doi.org/10.1021/ol101618u

2. Metal-Free Regioselective Oxidative Biaryl Coupling Leading to Head-to-Tail Bithiophenes: Reactivity Switching, a Concept Based on the Iodonium(III) Intermediate
Koji Morimoto, Nobutaka Yamaoka, Chieko Ogawa, Tomofumi Nakae, Hiromichi Fujioka, Toshifumi Dohi and Yasuyuki Kita
Org. Lett., Article ASAP

DOI:

http://dx.doi.org/10.1021/ol101498r

3. Rhodium-Catalyzed Oxidative C-H Arylation of 2-Arylpyridine Derivatives via Decarbonylation of Aromatic Aldehydes
Qi Shuai, Luo Yang, Xiangyu Guo, Olivier Basl and Chao-Jun Li
J. Am. Chem. Soc., Article ASAP

DOI:

http://dx.doi.org/10.1021/ja105396b

4. Cobalt-Catalyzed Hydroarylation of Alkynes through Chelation-Assisted C-H Bond Activation
Ke Gao, Pin-Sheng Lee, Takeshi Fujita and Naohiko Yoshikai
J. Am. Chem. Soc., Article ASAP

DOI:

http://dx.doi.org/10.1021/ja106814p

5. Competitive Carbon?Sulfur vs Carbon?Carbon Bond Activation of 2-Cyanothiophene with [Ni(dippe)H]2
Matthew R. Grochowski, Ting Li, William W. Brennessel and William D. Jones
J. Am. Chem. Soc., Article ASAP

DOI:

http://dx.doi.org/10.1021/ja104158h

6. Copper-Catalyzed Aerobic Oxidative Functionalization of an Arene C-H Bond: Evidence for an Aryl-Copper(III) Intermediate
Amanda E. King, Lauren M. Huffman, Alicia Casitas, Miquel Costas, Xavi Ribas and Shannon S. Stahl
J. Am. Chem. Soc., Article ASAP

DOI:

http://dx.doi.org/10.1021/ja1045378

7. Organocatalysis in Cross-Coupling: DMEDA-Catalyzed Direct C-H Arylation of Unactivated Benzene
Wei Liu, Hao Cao, Hua Zhang, Heng Zhang, Kin Ho Chung, Chuan He, Haibo Wang, Fuk Yee Kwong and Aiwen Lei
J. Am. Chem. Soc., Article ASAP

DOI:

http://dx.doi.org/10.1021/ja103050x

8. Direct Synthesis of 6-Arylpurines by Reaction of 6-Chloropurines with Activated Aromatics
Hai-Ming Guo, Pu Li, Hong-Ying Niu, Dong-Chao Wang and Gui-Rong Qu
J. Org. Chem., Article ASAP

DOI:

http://dx.doi.org/10.1021/jo1010334

9. Synthesis and Reactivity of NiII(Phpy)2 (Phpy = 2-Phenylpyridine)
Andrew T. Higgs, Paul J. Zinn and Melanie S. Sanford
Organometallics, Article ASAP

DOI:

http://dx.doi.org/10.1021/om100387z

10. Assembly of Symmetrical or Unsymmetrical Cyclometalated Organoplatinum Complexes through a Bridging Diphosphine Ligand
S. Masoud Nabavizadeh, Mohsen Golbon Haghighi, Ahmad R. Esmaeilbeig, Fatemeh Raoof, Zeinab Mandegani, Sirous Jamali, Mehdi Rashidi and Richard J. Puddephatt
Organometallics, Article ASAP

DOI:

http://dx.doi.org/10.1021/om100295q

11. Novel, Very Strong, Uncharged Auxiliary Bases; Design and Synthesis of Monomeric and Polymer-Bound Triaminoiminophosphorane Bases of Broadly Varied Steric Demand
Reinhard Schwesinger,Jürgen Willaredt, Helmut Schlemper, Manfred Keller, Dieter Schmitt, Hans Fritz
Chemische Berichte
Volume 127, Issue 12, pages 2435–2454

DOI:

http://dx.doi.org/10.1002/cber.19941271215

12. Extremely Strong, Uncharged Auxiliary Bases; Monomeric and Polymer-Supported Polyaminophosphazenes (P2–P5)
Reinhard Schwesinger, Helmut Schlemper, Christian Hasenfratz, Jürgen Willaredt, Tim Dambacher, Thomas Breuer, Carol Ottaway, Michael Fletschinger, Joachim Boele, Hans Fritz, Dietmar Putzas, Heinz W. Rotter, Frederick G. Bordwell, Amruthur V. Satish, Guo-Zen Ji, Eva-Maria Peters, Karl Peters, Hans Georg von Schnering, Leonhard Walz
Liebigs Annalen
Volume 1996, Issue 7, pages 1055–1081

DOI:

http://dx.doi.org/10.1002/jlac.199619960705

[petrovps]

iga22, оформите согласно правилам

[iga22]

iga22, оформите согласно правилам

Прошу прошения, не могли бы Вы конкретней указать на мною допущенные недочеты в составлении запроса. Я только что несколько раз перечитал правила оформления и ни нашел никаких несоответствий.....

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Если ВЫ про страницы, том и выпуск, то там стоит ASAP

[Himera]

1,2

[iga22]

Спасибо, Himera!!!

[хрюк]

С 3 по 10:

[iga22]

Спасибо, хрюк!!!

остались номер 3, 11 и 12

[macro]

11,12

[iga22]

Спасибо, macro!!!

осталcя номер 3, хрюк вылозил с 4 по 10, а 3 пропустил.....

[хрюк]

А вот и № 3: