Abstract:
Highly efficient processes are provided for preparing key intermediates in the synthesis of compounds (I). The process are broadly applicable and can provide selected components having a variety of substituents. Some intermediates are claimed.
Abstract:
The invention generally relates to improved processes for the preparation of intermediates of a cyclic dinucleotide which is useful as a STING agonist.
Abstract:
An improved process for making a compound B of the structure wherein n, R1, R2, and R3 are as defined in the specification. Compound B can be used to make tubulysin analogs that are, in turn, useful as anti-cancer agents, particularly when deployed in an antibody-drug conjugate.
Abstract:
The invention generally relates to improved processes for the preparation of intermediates of a cyclic dinucleotide which is useful as a STING agonist.
Abstract:
A process for making the compound of Formula I utilizes the starting compound, together with sulfilimine and sulfoxide process steps later on.
Abstract:
A process for making the compound of Formula I utilizes the starting compound, together with sulfilimine and sulfoxide process steps later on.