333354-29-3

Upstream product

• 756899-95-3 (2R,3S,4S)-1-benzyloxy-2,4-dimethyl-6-(tert-butyldiphenylsilyloxy)-3-hexanol 
• 134961-82-3 (2R,3S,4S)-1-benzyloxy-2,4-dimethyl-3,6-hexanediol 
• 108814-35-3 (2R,3R,4S)-1-(benzyloxy)-2,4-dimethyl-3-hydroxy-5-hexene 
• 756899-97-5 (2S,4R)-1-benzyloxy-6-(tert-butyldiphenylsilyloxy)-2,4-dimethylhexane 
• 333354-13-5 ((2S,4R)-2,4-Dimethyl-hex-5-enyloxymethyl)-benzene 
• 756899-96-4 (2R,3S,4S)-O-phenyl-3-[1-benzyloxy-2,4-dimethyl-6-(tert-butyldiphenylsilyloxy)-hexyl]thiocarbonate 

Downstream Products

• 756900-22-8 Methanesulfonic acid (3R,5S)-6-benzyloxy-3,5-dimethyl-hexyl ester 
• 756899-98-6 (2S,4R)-5-azido-1-benzyloxy-2,4-dimethylhexane 
• 756900-23-9 (3R,5S)-6-Benzyloxy-3,5-dimethyl-hexylamine 
• 756899-99-7 (2S)-N-((3R,5S)-3,5-dimethyl-6-benzyloxyhexyl)-2-methylbutyramide 
• 247184-89-0 (3R,7S,8S,10R,2'S)-kalkitoxin 
• 247184-89-0 (3R,7R,8S,10R,2'S)-kalkitoxin 

Relevant academic research and scientific papers

Synthesis of C3-C21 Segment of Aflastatin A Using Remote Asymmetric Induction Reactions

The C3-C21 segment of aflastatin A has been synthesized by converging three segments including the C3-C8 segment, the C9-C15 segment, and the C16-C21 segment. Each segment has been synthesized from a vinylketene silyl N,O-acetal possessing a chiral auxili

An expeditious total synthesis of kalkitoxins: Determination of the absolute stereostructure of natural kalkitoxin

Kalkitoxin, a potent neurotoxin isolated from the marine cyanobacteria Lyngbya majuscula, and its congeners (1-7) were efficiently synthesized utilizing Hruby's diastereoselective 1,4-addition and the Wipf's oxazoline-thiazoline conversion as key steps. T

Total synthesis of antitumor depsipeptide (-)-doliculide.

[reaction: see text] (-)-Doliculide, a potent antitumor agent, is synthesized stereoselectively in a convergent manner. The key strategy involves a stereoselective synthesis of the polyketide unit and synthesis of the D-tyrosine derivative, followed by as