A. Pfizenmayer

发表

Inhibition of protein synthesis by didemnins: cell potency and SAR.

P. Toogood, M. Joullié, D. Beidler, 2000, Journal of medicinal chemistry.

Synthesis and biological activities of [N-MeLeu5]- and [N-MePhe5]-didemnin B

M. Joullié, X. Ding, D. Xiao, 1999 .

Synthesis and biological activity of [Tic5] didemnin B.

W. Chen, M. Joullié, D. Xiao, 1998, Bioorganic & medicinal chemistry letters.

Synthesis and biological activities of [N-MeLeu5] didemnin B

Wei-Chuan Chen, M. Joullié, X. Ding, 1996 .

Synthesis of New Didemnin B Analogs for Investigations of Structure/Biological Activity Relationships

S. Mayer, M. Joullié, M. Vera, 1994 .

Synthetic studies of a constrained ring didemnin analog

Wen-Ren Li, M. Joullié, A. Pfizenmayer, 1994 .

Total syntheses of conformationally constrained didemnin B analogues. replacements of N,O-dimethyltyrosine with L-1,2,3,4-tetrahydroisoquinoline and L-1,2,3,4-tetrahydro-7-methoxyisoquinoline.

J. Tarver, M. Joullié, A. Pfizenmayer, 2001, The Journal of organic chemistry.

[Lys3]Didemnins as potential affinity ligands.

M. Joullié, D. Xiao, M. Vera, 2001, Bioorganic & medicinal chemistry letters.

Stereoselective synthesis of a conformationally restricted β-hydroxy-λ-amino acid

P. Carroll, M. Joullié, D. Xiao, 1997 .