+++J.Med.Chem, JACS, & some other (9)

[Psi_X]

Извените за наглось, если не сложно:
1. European Journal of Medicinal Chemistry, Volume 30, Issue 5, 1995, Pages 415-421
New 2-pyridylethylamines with dopaminergic activity: Synthesis and radioligand-binding evaluation
Claudi, F.; Cingolani, G. M.; Giorgioni, G.; Cardellini, M.; Amenta, F.; Polidori, C.

Код: Выделить всё

http://dx.doi.org/10.1016/0223-5234(96)88251-1

2. J. Med. Chem., 1998, 41 (6), pp 877–893
Inhibitors of Farnesyl Protein Transferase. 4-Amido, 4-Carbamoyl, and 4-Carboxamido Derivatives of 1-(8-Chloro-6,11-dihydro-5H-benzo[5,6]- cyclohepta[1,2-b]pyridin-11-yl)piperazine and 1-(3-Bromo-8-chloro-6,11- dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)piperazine
Alan K. Mallams,* Randall R. Rossman, Ronald J. Doll, Viyyoor M. Girijavallabhan, Ashit K. Ganguly, Joanne Petrin, Lynn Wang, Robert Patton,

Код: Выделить всё

http://dx.doi.org/10.1021/jm970462w

3. European Journal of Medicinal Chemistry, Volume 34, Issue 2, February 1999, Pages 177-190
Synthesis and binding of 6,7,8,9-tetrahydro-5H-pyrido[3,4-d]azepine and related ring-opened analogs at central nicotinic receptors
un-Xing Chenga, Malgorzata Dukata, Matthew Dowd

Код: Выделить всё

http://dx.doi.org/10.1016/S0223-5234(99)80051-8

4. J. Med. Chem., 2001, 44 (26), pp 4716–4732
Dopamine D3 Receptor Antagonists. 1. Synthesis and Structure−Activity Relationships of 5,6-Dimethoxy-N-alkyl- and N-Alkylaryl-Substituted 2-Aminoindans
Susanne R. Haadsma-Svensson,*† Kerry A. Cleek,† Dac M. Dinh,† J. Neil Duncan

Код: Выделить всё

http://dx.doi.org/10.1021/jm010145w

5. J. Med. Chem., 2003, 46 (25), pp 5458–5470
Nα-Imidazolylalkyl and Pyridylalkyl Derivatives of Histaprodifen: Synthesis and in Vitro Evaluation of Highly Potent Histamine H1-Receptor Agonists
Sonja Menghin,† Heinz H. Pertz,*† Kai Kramer,† Roland Seifert,‡ Walter Schunack,† and Sigurd Elz

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http://dx.doi.org/10.1021/jm0309147

6. J. Am. Chem. Soc., 1955, 77 (3), pp 675–683
Synthesis of Dimethylapoerysopine and an Approach to the Total Synthesis of the Unrearranged Erythrina Bases
K. Wiesner, Z. Valenta, A. J. Manson, F. W. Stonner

Код: Выделить всё

http://dx.doi.org/10.1021/ja01608a040

7. J. Am. Chem. Soc., 1980, 102 (15), pp 5036–504
Reactions of 4a-peroxides and 4a-pseudobases of N10- and N5-phenethylflavins
Masaki Iwata, Thomas C. Bruice, H. L. Carrell, Jenny P. Glusker

Код: Выделить всё

http://dx.doi.org/10.1021/ja00535a035

8. J. Med. Chem., 1985, 28 (2), pp 225–233
Substituted 5H-dibenz[b,g]-1,4-oxazocines and related amino acids with antiinflammatory activity
Michael R. Stillings, Stephen Freeman, Peter L. Myers, Michael J. Readhead

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http://dx.doi.org/10.1021/jm00380a013

9. Synthetic Communications, Volume 38, Issue 11 January 2008 , pages 1822 - 1829
A New Route of Synthesis of 5-(N-Phenethylamino)salicylic Acid Derivatives by Rapid and Selective Reduction of the Amide Group with NaBH4/Acetic Acid
Young-Gyun Shin a; Ho-Joon Park a; HaeUn Lee a; Sung-Hwa Yoon

Код: Выделить всё

http://dx.doi.org/10.1080/00397910801982001

за ранее огроменное спасибо!

[Elvira]

3

[VOVAN CIR]

9

[Elvira]

1

[mercaptan]

2,4,5,8

[Marxist]

6, 7

[Psi_X]

усем спасибо, огромное человеческое спасибо!!!!