Download PDF by Clemens Lamberth, J?rgen Dinges: Bioactive carboxylic compound classes: pharmaceuticals and

By Clemens Lamberth, J?rgen Dinges

ISBN-10: 3527339477

ISBN-13: 9783527339471

ISBN-10: 3527693939

ISBN-13: 9783527693931

ISBN-10: 3527693947

ISBN-13: 9783527693948

ISBN-10: 3527693955

ISBN-13: 9783527693955

ISBN-10: 3527693963

ISBN-13: 9783527693962

Following the winning and confirmed idea utilized in "Bioactive Heterocyclic Compound sessions" through an analogous editors, this ebook is the 1st to give licensed pharmaceutical and agrochemical compounds labeled via their carboxylic acid performance in a single convenient volume.
all the round forty chapters describes one or standard syntheses of a selected compound classification and gives concise details at the heritage of improvement, mode of motion, organic job and box of software, in addition to structure-activity relationships. additionally, similarities and variations among prescription drugs and agrochemicals are mentioned within the creation.
Written by means of a workforce of specialists within the box, it is a helpful reference for researchers in academia and chemical or pharmaceutical businesses operating within the box of overall synthesis and usual product chemistry, drug improvement, and crop defense learn

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Additional resources for Bioactive carboxylic compound classes: pharmaceuticals and agrochemicals

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27, 147–149. G. (1990) J. Med. , 33, 2876–2882. A. H. (1979) N-(4-Piperidinyl)-N-phenylamides, US Patent 4179569. 19. L. F. (1990) J. Org. , 55, 4207–4209. 20. J. -L. , 55, 501–502. 21. , and 22. 23. 24. 25. 26. 27. 28. 29. 30. 31. 32. 33. 34. Carroll, R. (2008) Improved method of making sufentanil, WO Patent 5423. , and Laconde, G. , 51, 2983–2985. , and Sadri, M. , 21, 71–82. , and Dai, R. (2011) Method for preparing lidocaine from 2,6-dimethylaniline and chloroacetyl chloride, CN Patent 102070483.

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While an increased hydrophobicity References improved tonic block (7 vs 40), extension of the carbonyl-amine proximity caused an opposite effect although having equal logP (40 vs 41) [39]. References 1. H. (2014) J. Pain, 15, 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. 1215–1226. H. I. J. N. Westhorpe), Springer-Verlag, New York, pp. 641–659. S. J. (2014) Future Med. , 6, 385–412. K. I. (2007) J. Med. , 50, 2583–2588. B. (2010) J. Clin. Pharm. , 35, 617–638. -J. (2002) Pharm. Unserer Zeit, 31, 13–22.

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Bioactive carboxylic compound classes: pharmaceuticals and agrochemicals by Clemens Lamberth, J?rgen Dinges


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