100950-87-6

Upstream product

• 1589-60-2 1-phenylcyclohexanol 
• 762-72-1 allyl-trimethyl-silane 
• 1444-65-1 (RS)-2-phenylcyclohexanone 

Downstream Products

• 108011-19-4 (1-phenyl-cyclohexyl)-acetaldehyde 
• 1356465-15-0 4-(1-phenylcyclohexyl)butanoic acid 
• 1356465-13-8 1-phenylcyclohexanebutanoic acid ethyl ester 
• 1356465-11-6 (E)-ethyl 4-(1-phenylcyclohexyl)but-2-enoate 
• 108667-56-7 3-(1-phenyl-cyclohexyl)-propane-1,2-diol 

Relevant academic research and scientific papers

Carbenium ion formation by fragmentation of electrochemically generated oxonium ions

Fragmentation of electrochemically generated oxonium ions can be exploited to form carbenium ions at a low oxidation potential in the presence of a nucleophile. The application of this concept is demonstrated for the allylation of carbenium ions generated by the anodic oxidation of stannylmethylethers.

SUBSTITUTED 3-PHENYL-1,2,4-OXADIAZOLE COMPOUNDS

Disclosed are compounds of Formula (I): (I) or stereoisomers, salts, or prodrugs thereof, wherein: (i) R1 and R2 are independently C1-C4 alkyl, or (ii) R1 and R2 together with the carbon atom to which they are a

SUBSTITUTED OXADIAZOLE COMPOUNDS AND THEIR USE AS S1P1 AGONISTS

Disclosed are compounds of Formula (I): [PLEASE INSERT CHEMICAL STRUCTURE HERE] or stereoisomers, N-oxides, salts, or prodrugs thereof; wherein: Ring A is phenyl or 5- to 6-membered heteroaryl; (i) R1 and R2 are independently C1-C4 alkyl; or (ii) R1 and R

SYNTHETIC STUDIES OF MARINE ALKALOIDS HAPALINDOLES. Part 1. TOTAL SYNTHESIS OF (+/-)-HAPALINDOLES J and M

The first concise synthesis of marine indole alkaloids (+/-) hapalindoles J (4) and M (5) was achieved in seven or six steps starting from a readily available compound 6 using important key reactions, 6 -> 7 -> 8 and 35 -> 41 or 5.