845784-35-2

Upstream product

• 210880-88-9 N-(tert-butoxycarbonyl)-3,5-dibromo-4-hydroxy-β-phenethylamine 
• 250284-68-5 2-bromo-4-(2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-phenol 
• 77251-51-5 Bis-(2-benzyloxy-5-formyl-phenyl)-iodonium; bromide 
• 845784-34-1 C₄₈H₄₁Br₃N₄O₈ 
• 845784-33-0 2-benzyloxyimino-3-(4-{5-[2-benzyloxyimino-2-(2-{3-[2-bromo-4-(2-tert-butoxycarbonylamino-ethyl)-phenoxy]-4-hydroxy-phenyl}-ethylcarbamoyl)-ethyl]-3-bromo-2-tert-butoxycarbonyloxy-phenoxy}-3-bromo-phenyl)-propionic acid tert-butyl ester 
• 845784-16-9 2-benzyloxyimino-3-{3-[4-(2-benzyloxyimino-2-tert-butoxycarbonyl-ethyl)-2-bromo-phenoxy]-5-bromo-4-tert-butoxycarbonyloxy-phenyl}-propionic acid 
• 845784-15-8 2-benzyloxyimino-3-{3-[4-(2-benzyloxyimino-2-tert-butoxycarbonyl-ethyl)-2-bromo-phenoxy]-5-bromo-4-tert-butoxycarbonyloxy-phenyl}-propionic acid methyl ester 
• 845784-12-5 3-[4-(2-Benzyloxy-5-{2-[(E)-benzyloxyimino]-2-methoxycarbonyl-ethyl}-phenoxy)-3-bromo-phenyl]-2-[(Z)-benzyloxyimino]-propionic acid 
• 845784-14-7 3-[4-(2-Benzyloxy-5-{2-[(E)-benzyloxyimino]-2-methoxycarbonyl-ethyl}-phenoxy)-3-bromo-phenyl]-2-[(E)-benzyloxyimino]-propionic acid 
• 845784-11-4 3-[4-Benzyloxy-3-(4-{2-[(Z)-benzyloxyimino]-3-hydroxy-propyl}-2-bromo-phenoxy)-phenyl]-2-[(E)-benzyloxyimino]-propionic acid methyl ester 
• 845784-10-3 3-[4-Benzyloxy-3-(4-{2-[(E)-benzyloxyimino]-3-hydroxy-propyl}-2-bromo-phenoxy)-phenyl]-2-[(E)-benzyloxyimino]-propionic acid methyl ester 
• 845784-00-1 2-[(E)-Benzyloxyimino]-3-[4-(5-{2-[(E)-benzyloxyimino]-2-methoxycarbonyl-ethyl}-3-bromo-2-hydroxy-phenoxy)-3-bromo-phenyl]-propionic acid 
• 845784-13-6 2-[(E)-Benzyloxyimino]-3-[4-(5-{2-[(E)-benzyloxyimino]-2-methoxycarbonyl-ethyl}-2-hydroxy-phenoxy)-3-bromo-phenyl]-propionic acid 
• 845784-52-3 {2-[4-(2-benzyloxy-5-cyanomethyl-phenoxy)-3,5-dibromo-phenyl]-ethyl}-carbamic acid tert-butyl ester 

Downstream Products

• 184679-29-6 bastadin 20 

Relevant academic research and scientific papers

A general method for the synthesis of bastaranes and isobastaranes: First total synthesis of bastadins 5, 10, 12, 16, 20, and 21

A general strategy for the synthesis of twenty naturally occurring bastadins (all but bastadin 3) is presented. A key retrosynthetic disconnection of the two amide bonds, common in all target molecules, bisects the macrocyclic core into two diaryl ether f