214978-16-2

Upstream product

• 91142-50-6 4-benzyloxy-2-butyn-1-ol 
• 124-63-0 methanesulfonyl chloride 
• 100-39-0 benzyl bromide 

Downstream Products

• 866825-08-3 2-(4-benzyloxy-2-butynyl)malonic acid dimethyl ester 
• 214978-22-0 (2S,3S)-3-Methyl-2-(trityl-amino)-pentanoic acid (4-benzyloxy-but-2-ynyl)-amide 
• 214978-23-1 N-(4-benzyloxy-but-2-ynyl)-benzamide 
• 214978-20-8 4-benzyloxy-but-2-ynylamine 
• 915969-13-0 2-(4-Benzyloxy-but-2-ynyl)-2-[(E)-3-((1R,2S)-2-hydroxymethyl-cyclopropyl)-but-2-enyl]-malonic acid dimethyl ester 
• 866825-13-0 ((3aS,7S)-8-(benzyloxymethyl)-7-((tert-butyldimethylsilyloxy)methyl)-2-methanesulfonyloxymethyl-4-methyl-1,2,3,3a,6,7-hexahydroazulen-2-yl)-methyl methanesulfonate 
• 866825-12-9 (3aS,7S)-dimethyl 8-((benzyloxy)methyl)-3,3a,6,7-tetrahydro-7-[(t-butyldimethylsiloxy)methyl]-4-methylazulene-2,2(1H)-dicarboxylate 
• 915969-17-4 [(3aS,7S)-8-Benzyloxymethyl-7-(tert-butyl-dimethyl-silanyloxymethyl)-2-hydroxymethyl-4-methyl-1,2,3,3a,6,7-hexahydro-azulen-2-yl]-methanol 
• 915969-15-2 2-(4-benzyloxy-but-2-ynyl)-2-[3-(2S,3S)-(2-carboxycyclopropyl)-but-2-enyl]malonic acid dimethyl ester 

Relevant academic research and scientific papers

Enantioselective syntheses of tremulenediol A and tremulenolide A

A concise entry to the skeleton of the tremulane sesquiterpenes is described that culminated in the first enantioselective syntheses of tremulenediol A and tremulenolide A. The approach features a series of efficient transition metal-catalyzed reactions c

Enantioselective syntheses of tremulenediol A and tremulenolide A

(Chemical Equation Presented) An enantioselective entry to the skeleton of the tremulane sesquiterpenes is described. The approach features a series of efficient transition metal-catalyzed reactions commencing with an enantioselective rhodium(II)-catalyze

Electrophilic fluorodesilylation of allenylmethylsilanes: A novel entry to 2-fluoro-1,3-dienes

(Chemical Equation Presented) Various fluorodienes were prepared by treatment of the corresponding allenylmethylsilanes with Selectfluor. This is the first route to these compounds not based on the use of a fluorinated building block. The reaction allows