Application
Used to prepare a SEM-ether which was, in turn, removed with BBr3 and cyclized to a benzo-oxapane.
Phenol protecting group in the synthesis of laterifluorones.
Features and Benefits
Convenient hydroxyl-protecting reagent. SEM-ethers are stable over a wide pH range, and can be selectively cleaved with fluoride ion under mild aprotic conditions.
General description
Learn More at the Professor and Product Portal of Professor Bruce Lipshutz.
Packaging
1, 5, 25, 100 g in glass bottle
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