95531-99-0

Upstream product

• 113219-30-0 (E)-5-Benzyloxy-2-methyl-pent-2-enoic acid ethyl ester 
• 95532-05-1 (E)-5-Benzyloxy-2-methyl-pent-2-enal 
• 4799-68-2 3-benzyloxypropan-1-ol 
• 100-39-0 benzyl bromide 
• 54314-84-0 1-[(3-bromopropoxy)methyl]-benzene 
• 54314-85-1 (3-benzyloxypropyl)triphenylphosphonium bromide 
• 19790-60-4 3-Benzyloxypropanal 

Downstream Products

• 95531-81-0 3-(benzyloxy)-1-bromo-2-methyl-2(E)-hexene 
• 95532-05-1 (E)-5-Benzyloxy-2-methyl-pent-2-enal 
• 947539-68-6 C₁₃H₁₈O₃ 
• 538350-19-5 (E)-7-Benzyloxy-2,4-dimethyl-hept-4-en-3-ol 
• 538350-20-8 (R)-1-[(2R,3R)-3-(2-Benzyloxy-ethyl)-2-methyl-oxiranyl]-2-methyl-propan-1-ol 
• 538350-21-9 (3R,5R)-1-Benzyloxy-6-methyl-4-methylene-heptane-3,5-diol 
• 1025949-33-0 tert-Butyl-[2-((4R,5S,6R)-6-isopropyl-2,2,5-trimethyl-[1,3]dioxan-4-yl)-ethoxy]-diphenyl-silane 
• 95531-82-1 (1S,4aS,8aR)-3-((E)-5-Benzyloxy-2-methyl-pent-2-enyloxy)-1-(tert-butyl-dimethyl-silanyloxymethyl)-8a-methyl-1,4,4a,5,6,7,8,8a-octahydro-naphthalene-2-carboxylic acid methyl ester 
• 503620-04-0 (2S,3S)-5-(benzyloxy)-2-methylpentane-1,3-diol 
• 107574-35-6 2-[(5E,9E)-12-Benzyloxy-5,9-dimethyl-2-(5-methyl-1-methylene-hex-4-enyl)-dodeca-5,9-dienyl]-[1,3]dioxolane 
• 107554-00-7 2-<(E,E)-10-(benzyloxy)-3,7-dimethyl-5-(phenylthio)-3,7-decadienyl>-1,3-dioxolane 
• 107553-97-9 (2E,6E,10E)-13-Benzyloxy-6,10-dimethyl-2-(4-methyl-pent-3-enyl)-trideca-2,6,10-trienoic acid ethyl ester 
• 107554-05-2 (6E,10E)-13-Benzyloxy-6,10-dimethyl-3-(5-methyl-1-methylene-hex-4-enyl)-trideca-6,10-dienal 
• 107553-98-0 (2E/Z,6E,10E)-13-(benzyloxy)-6,10-dimethyl-2-(4-methyl-3-pentenyl)-2,6,10-tridecatrien-1-ol 

Relevant academic research and scientific papers

Synthesis of the C17-C25 subunit of lasonolide A utilizing a Tsuchihashi-Yamamoto type rearrangement

An efficient synthesis of the C17-C25 subunit resident in (-)-lasonolide A is reported herein. The key reaction features that were utilized include a Tsuchihashi-Yamamoto type rearrangement and Molander-Reformatsky SmI2 me

Synthesis of (+)-prelactone B

Radical-mediated opening of a trisubstituted epoxy alcohol using cp2TiCl was followed by diastereoselective reduction of the resulting product with a centrally located methylene group, flanked on both sides by two chiral hydroxyl-bearing carbon

SYNTHESIS OF MACROCYCLIC TERPENOIDS BY INTRAMOLECULAR CYCLIZATION X. TOTAL SYNTHESIS OF METHYL CERIFERATE-I

The methyl ester of (+/-)-ceriferic acid-I, a 14-membered ring sesterterpene isolated from the wax of the scale insect Ceroplastes ceriferus, was synthesized by means of an intramolecular Wittig-type reaction.