Vivi Pant
Chem Soc Rev
Nucleophilic Acyl Substitutions of Anhydrides with Protic Nucleophiles Catalyzed by Amphoteric, Oxomolybdenum Species | The Journal of Organic Chemistry
Efficient and Practical Procedure for the Esterification of the Free α-Car- boxylic Acid of Amino Acid Residues with β-(Trimet
PDF) Versatile selective α-carboxylic acid esterification of N-protected amino acids and peptides by alcalase
Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products - Natural Product Reports (RSC Publishing) DOI:10.1039/C4NP00106K
Nucleophilic Acyl Substitutions of Anhydrides with Protic Nucleophiles Catalyzed by Amphoteric, Oxomolybdenum Species | The Journal of Organic Chemistry
Convenient Synthesis of N-Methylamino Acids Compatible with Fmoc Solid-Phase Peptide Synthesis | The Journal of Organic Chemistry
Characterization of novel heterocyclic compounds based on 4-aryl-4H-chromene scaffold as anticancer agents: Design, synthesis, antiprofilerative activity against resistant cancer cells, dual β-tubulin/c-Src inhibition, cell cycle arrest and apoptosis ...
Synthesis of Microcolin B, a Potent New Immunosuppressant Using an Efficient Mixed Imide Formation Reaction | The Journal of Organic Chemistry
Frontiers | Recent Approaches to the Identification of Novel Microtubule-Targeting Agents
CLIP-170 Highlights Growing Microtubule Ends In Vivo: Cell
Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products - Natural Product Reports (RSC Publishing) DOI:10.1039/C4NP00106K
Acne Studios for Women SS23 Collection | SSENSE
Wool Blend Long Coat | UNIQLO US
PDF) Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products
Designer Flared Pants - FARFETCH
The ester derivatives obtained by C-ring modification of podophyllotoxin induce apoptosis and inhibited proliferation in PC-3M cells via down-regulation of PI3K/Akt signaling pathway - ScienceDirect
Design, Synthesis and Antitumor Activity of Novel link-bridge and B-Ring Modified Combretastatin A-4 (CA-4) Analogues as Potent Antitubulin Agents | Scientific Reports
