Development and Large-Scale Preparation of an Oral TACE Inhibitor

Author:

Savage Scott A.1,Waltermire Robert E.1,Campagna Silvio1,Bordawekar Shailendra1,Dalla Riva Toma Joan1

Affiliation:

1. Bristol-Myers Squibb Company, Research and Development, One Squibb Drive, New Brunswick, New Jersey 08903, U.S.A.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference22 articles.

1. aMaduskuie, T. P., Jr., Duan, J., and Mercer, S. E.(Dupont Pharmaceuticals Company, U.S.A.).Novel Lactam Metalloprotease Inhibitors. PCT Int. Appl. WO 2002/004416 A2, 20020117, 2002.

2. bDuan, J. J.W., Chen, L., Lu, Z., Wasserman, Z. R., Maduskuie, T. P., Liu, R.Q., Covington, M. B., Vaddi, K. G., Qian, M., Voss, M. E., Xue, C.B., Hardman, K. D., Ribadeneira, M. D., Newton, R. C., Magolda, R. L., Christ, D. D., and Decicco, C. P.Abstracts of Papers;224th ACS National Meeting,Boston, MA, U.S.A.,August 18−22, 2002,American Chemical Society:Washington, DC, 2002, MEDI-426.

3. For reviews and syntheses of related tetra-substituted amino acids see:

4. Stereoselective synthesis of quaternary α-amino acids. Part 1: Acyclic compounds

5. Stereoselective synthesis of (S)-(+)-αM4CPG, a selective antagonist of metabotropic glutamate receptors

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