920749-75-3

Upstream product

• 920749-68-4 (Z)-(S)-7-Benzyloxy-1-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl)-3-(3-triisopropylsilanyloxy-propyl)-hept-2-en-1-ol 
• 3019-71-4 Trichloroacetyl isocyanate 
• 80434-59-9 (1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxaldehyde 

Downstream Products

• 920750-13-6 [(S)-5-Benzyloxy-1-[(E)-2-((1S,2S,5R)-2-isopropyl-5-methyl-cyclohexyl)-vinyl]-1-(3-triisopropylsilanyloxy-propyl)-pentyl]-carbamic acid 9H-fluoren-9-ylmethyl ester 
• 920749-76-4 (S)-5-Benzyloxy-1-[(E)-2-((1S,2S,5R)-2-isopropyl-5-methyl-cyclohexyl)-vinyl]-1-(3-triisopropylsilanyloxy-propyl)-pentylamine 
• 920749-86-6 N-[(S)-5-Benzyloxy-1-[(E)-2-((1S,2S,5R)-2-isopropyl-5-methyl-cyclohexyl)-vinyl]-1-(3-triisopropylsilanyloxy-propyl)-pentyl]-acrylamide 

Relevant academic research and scientific papers

Cleavage of a chiral auxiliary using RCM on an especially sterically crowded alkene: Syntheses of chiral carbo- and heterocycles

Chiral 1,5-, 1,6-, and 1,7-dienes generated in 3-4 steps from chiral auxiliary p-menthane-3-carboxaldehyde undergo RCM with notable discrepancies in reactivity depending on the nature and number of substituents flanking the central double bond. The chiral