+++11 from ACS СПАСИБО, Biginelli!!!!

[Anhydride]

Очень надо статьи из ACS, пожалуйста, выложьте у кого возможность есть...

1. Synthesis of 2-Aminobenzoxazoles Using Tetramethyl Orthocarbonate or 1,1-Dichlorodiphenoxymethane
Christopher L. Cioffi, John J. Lansing, and Hamza Yüksel
J. Org. Chem., 2010, 75 (22), pp 7942–7945

Код: Выделить всё

http://dx.doi.org/10.1021/jo1017052

2. Capturing the Essence of Organic Synthesis: From Bioactive Natural Products to Designed Molecules in Today’s Medicine
Arun K. Ghosh
J. Org. Chem., 2010, 75 (23), pp 7967–7989

Код: Выделить всё

http://dx.doi.org/10.1021/jo101606g

3. Alumina-Supported Cu(II), A Versatile and Recyclable Catalyst for Regioselective Ring Opening of Aziridines and Epoxides and Subsequent Cyclization to Functionalized 1,4-Benzoxazines and 1,4-Benzodioxanes
Sukalyan Bhadra, Laksmikanta Adak, Subhas Samanta, A. K. M. Maidul Islam, Manabendra Mukherjee, and Brindaban C. Ranu
J. Org. Chem., 2010, 75 (24), pp 8533–8541

Код: Выделить всё

http://dx.doi.org/10.1021/jo101916e

4. Synthesis of Oxazolo[4,5-c]quinoline TRPV1 Antagonists
Eric A. Voight, Jerome F. Daanen, and Michael E. Kort
J. Org. Chem., 2010, 75 (24), pp 8713–8715

Код: Выделить всё

http://dx.doi.org/10.1021/jo101938b

5. Alkyl 4-Chlorobenzoyloxycarbamates as Highly Effective Nitrogen Source Reagents for the Base-Free, Intermolecular Aminohydroxylation Reaction
Lawrence Harris, Simon P. H. Mee, Richard H. Furneaux, Graeme J. Gainsford, and Andreas Luxenburger
J. Org. Chem., 2011, 76 (2), pp 358–372

Код: Выделить всё

http://dx.doi.org/10.1021/jo1018816

6. Asymmetric Synthesis of 1,2,9,9a-Tetrahydrocyclopropa[c]benzo[e]indol-4-one (CBI)
James P. Lajiness and Dale L. Boger
J. Org. Chem., 2011, 76 (2), pp 583–587

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http://dx.doi.org/10.1021/jo102136w

7. Catalytic Acylation of Amines with Aldehydes or Aldoximes
C. Liana Allen, Simge Davulcu, and Jonathan M. J. Williams
Org. Lett., 2010, 12 (22), pp 5096–5099

Код: Выделить всё

http://dx.doi.org/10.1021/ol101978h

8. Palladium-Catalyzed Domino Ring-Opening/Carboxamidation Reactions of N-Tosyl Aziridines and 2-Iodothiophenols: A Facile and Efficient Approach to 1,4-Benzothiazepin-5-ones
Fanlong Zeng and Howard Alper
Org. Lett., 2010, 12 (23), pp 5567–5569

Код: Выделить всё

http://dx.doi.org/10.1021/ol102394h

9. Green Progression for Synthesis of Regioselective β-Amino Alcohols and Chemoselective Alkylated Indoles
Boningari Thirupathi, Rapelli Srinivas, Avvari N. Prasad, J. K. Prashanth Kumar, and Benjaram M. Reddy
Org. Process Res. Dev., 2010, 14 (6), pp 1457–1463

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http://dx.doi.org/10.1021/op1002177

10. A Kilolaboratory Preparation of the CNRS Chiral Auxiliary
Nathan R. Guz, Matt Pfeiffer, and Dan Dickman
Org. Process Res. Dev., 2010, 14 (6), pp 1476–1478

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http://dx.doi.org/10.1021/op1002227

11. Kinetic and Scale-Up Investigations of Epoxide Aminolysis in Microreactors at High Temperatures and Pressures
Nikolay Zaborenko, Matthew W. Bedore, Timothy F. Jamison, and Klavs F. Jensen
Org. Process Res. Dev., 2011, 15 (1), pp 131–139

Код: Выделить всё

http://dx.doi.org/10.1021/op100252m

СПАСИБО ОЧЕНЬ БОЛЬШОЕ ЗАРАНЕЕ!!!

[Biginelli]