Completion

After synthesizing the C(38)-C(54) subunit, it can be used as a key intermediate for further assembly into the complete molecule, halichondrin B.

If you need to purchase chemical raw materials, submit your demand information to get the latest quotations.

An expeditious synthesis of the C(38)-C(54) halichondrin B subunit
Related Chemicals
- (S,E)-1-(benzyloxy)hex-4-en-3-ol
Consecutive sigmatropic rearrangements in the enantioselective total synthesis of (-)-joubertinamine and (-)-mesembrine
Related Chemicals
- methyl 2-(3,4-dimethoxyphenyl)hex-5-enoate
Total Synthesis of Pterocarpan: (+/-)-Neorautenane
Related Chemicals
- (7aR,13aR)-3,3-dimethyl-7a,13a-dihydro-3H,7H-[1,3]dioxolo[5,6][1]benzofuro[3,2-c]pyrano[3,2-g]chromene

Characterization Stereoselective synthesis Protecting groups Purification Isolation and Purification Starting Material Retrosynthetic analysis Purification and characterization Final steps Final Deprotection Ring Formation Intermediate Formation Construction of Fragments Assembly Optimization and Troubleshooting Functional Group Introduction C-C Bond Formation Key Sigmatropic Rearrangements Sequential Transformations Oxidation/Reduction Reactions

Chemical Baike