130486-37-2

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 130486-36-1 ((1R,2S)-2-Hydroxymethyl-cyclopentyl)-acetic acid tert-butyl ester 
• 119729-72-5 (E)-methyl-6-hydroxy-hex-2-en-oate 
• 130486-34-9 (E)-6-(Toluene-4-sulfonyloxy)-hex-2-enoic acid methyl ester 
• 130486-35-0 (1S,2R)-2-tert-Butoxycarbonylmethyl-cyclopentanecarboxylic acid methyl ester 
• 77823-74-6 (E)-6-Iod-2-hexensaeure-methylester 
• 127089-43-4 (E)-methyl-6-[(tetrahydro-2H-pyran-2-yl)oxy]-hex-2-en-oate 
• 150942-98-6 t-butyl lithioacetate 

Relevant academic research and scientific papers

SYNTHESIS OF IKARUGAMYCIN: MODEL STUDIES ON A NEW STRATEGY FOR THE CLOSURE OF RING C

A new conjugated addition-alkylation approach suitable for the closure or ring C of ikarugamycin is demonstrated by the concise elaboration of a trans-disubstituted cyclopentane that has been converted into the cyclopentane analogue of the natural product