Compound 4 was prepared from 3 using LgdB1 [13 (link)]. A 125-mL reaction mixture containing 2.0 g of 3 (not completely dissolved at the start of the reaction due to its low solubility) and 0.36 mg LgdB1 in 10 mM Tris-HCl buffer (pH 7.5) was rotary-shaken (150 rpm) at 30 °C for 18 h. After the reaction, His6-tagged LgdB1 was removed by adding 1 mL of Nuvia IMAC Ni-charged Resin (Bio-Rad Laboratories, Inc. Hercules, CA, USA) followed by filtration. The mixture was deionized by electrodialysis using a Microacylyzer S1 with an AC220-10 membrane cassette (Astom Corporation, Tokyo, Japan), concentrated to approximately 20 mL using a rotary evaporator, and lyophilized to obtain 1.89 g of 4 (yield 94 %).