134961-82-3

Upstream product

• 134961-80-1 2-((E)-(R)-5-Benzyloxy-2,4-dimethyl-pent-3-enyloxy)-tetrahydro-pyran 
• 134961-79-8 (E)-(R)-2,4-Dimethyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-en-1-ol 
• 134961-78-7 (E)-(R)-2,4-Dimethyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-enoic acid ethyl ester 
• 100-39-0 benzyl bromide 
• 74130-36-2 (E)-1-Benzyloxy-2,4-dimethyl-2-penten-5-ol 
• 108814-35-3 (2R,3R,4S)-1-(benzyloxy)-2,4-dimethyl-3-hydroxy-5-hexene 
• 134961-75-4 ((E)-(S)-2,4-Dimethyl-hexa-2,5-dienyloxymethyl)-benzene 

Downstream Products

• 333354-29-3 (3R,5S)-6-benzyloxy-3,5-dimethylhexanol 
• 756899-96-4 (2R,3S,4S)-O-phenyl-3-[1-benzyloxy-2,4-dimethyl-6-(tert-butyldiphenylsilyloxy)-hexyl]thiocarbonate 
• 756900-05-7 (4R)-4-phenyl-3-[(3R,4S,6R)-3,4,6-trimethyl-8-((2S)-N-methyl-2-methylbutyramido)-octanoyl]-2-oxazolidinone 
• 756900-17-1 (4S)-4-phenyl-3-[(3S,4S,6R)-3,4,6-trimethyl-8-((2S)-N-methyl-2-methylbutyramido)-octanoyl]-2-oxazolidinone 
• 756900-02-4 (4R)-phenyl-3-[(4R,6R)-4,6-dimethyl-8-((2S)-N-methyl-2-methylbutyramido)-(E)-2-octenoyl]-2-oxazolidinone 
• 756900-16-0 (4S)-phenyl-3-[(4R,6R)-4,6-dimethyl-8-((2S)-N-methyl-2-methylbutyramido)-(E)-2-octenoyl]-2-oxazolidinone 
• 756899-97-5 (2S,4R)-1-benzyloxy-6-(tert-butyldiphenylsilyloxy)-2,4-dimethylhexane 
• 247184-89-0 (3R,7R,8S,10R,2'S)-kalkitoxin 
• 247184-89-0 (3R,7S,8S,10R,2'S)-kalkitoxin 
• 756900-00-2 (2S)-N-methyl-N-((3R,5S)-3,5-dimethyl-6-benzyloxy-hexyl)-2-methylbutyramide 
• 756899-99-7 (2S)-N-((3R,5S)-3,5-dimethyl-6-benzyloxyhexyl)-2-methylbutyramide 
• 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 

Relevant academic research and scientific papers

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

Stereospecific construction of three contiguous asymmetric centers via cyclic hydroboration

Diastereospecific construction of three contiguous asymmetric centers assembled in optically active 1,4-diols, cyclopentanones, and δ-lactones have been achieved via A(1,3)-strain controlled cyclic hydroboration.