1. Academic Validation
  2. Streamlined Total Synthesis of Shishijimicin A and Its Application to the Design, Synthesis, and Biological Evaluation of Analogues thereof and Practical Syntheses of PhthNSSMe and Related Sulfenylating Reagents

Streamlined Total Synthesis of Shishijimicin A and Its Application to the Design, Synthesis, and Biological Evaluation of Analogues thereof and Practical Syntheses of PhthNSSMe and Related Sulfenylating Reagents

  • J Am Chem Soc. 2018 Sep 26;140(38):12120-12136. doi: 10.1021/jacs.8b06955.
K C Nicolaou Ruofan Li Zhaoyong Lu Emmanuel N Pitsinos 1 Lawrence B Alemany Monette Aujay 2 Christina Lee 2 Joseph Sandoval 2 Julia Gavrilyuk 2
Affiliations

Affiliations

  • 1 Laboratory of Natural Products Synthesis & Bioorganic Chemistry, Institute of Nanoscience and Nanotechnology , National Centre for Scientific Research "Demokritos" , 153 10 Agia Paraskevi , Greece.
  • 2 AbbVie Stemcentrx, LLC , 450 East Jamie Court , South San Francisco , California 94080 , United States.
Abstract

Shishijimicin A is a scarce marine natural product with highly potent cytotoxicities, making it a potential payload or a lead compound for designed antibody-drug conjugates. Herein, we describe an improved total synthesis of shishijimicin A and the design, synthesis, and biological evaluation of a series of analogues. Equipped with appropriate functionalities for linker attachment, a number of these analogues exhibited extremely potent cytotoxicities for the intended purposes. The synthetic strategies and tactics developed and employed in these studies included improved preparation of previously known and new sulfenylating reagents such as PhthNSSMe and related compounds.

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