36742-36-6

Usage

Structure

A derivative of benzene with a cyclopentenyl group and a methoxy group attached to the benzene ring.

Synonyms

1-(1-cyclopenten-1-yl)-3-methoxybenzene

Applications

Commonly used in organic synthesis and pharmaceutical research.

Potential uses

May have applications in the development of new drugs and other industrial products.

Relevance in organic chemistry

Its structure and reactivity make it an interesting target for further study in organic chemistry.

Ongoing research

Properties and potential uses are still being explored.

Upstream product

• 36282-40-3 (3-methoxyphenyl)magnesium bromide 
• 120-92-3 cyclopentanone 
• 66107-33-3 3-methoxyphenyl triflate 
• 142-29-0 cyclopentene 
• 2398-37-0 3-methoxyphenyl bromide 
• 142144-65-8 1-(3-methoxyphenyl) cyclopentan-1-ol 

Downstream Products

• 36744-81-7 1-(p-Methoxyphenyl)-1-(m-methoxyphenyl)-cyclopentan 
• 36744-82-8 4-[1-(3-methoxyphenyl)cyclopentyl]phenol 
• 75146-71-3 1-(3-methoxyphenyl)-6-oxabicyclo[3.1.0]hexane 
• 64417-35-2 2-Brom-5-(N-Carbethoxy-N-methylaminoethyl)-5-(3-methoxyphenyl)-cyclopent-2-enon 
• 64417-33-0 2-(N-Carbethoxy-N-methylaminoethyl)-2-(3-methoxyphenyl)-cyclopentanon 
• 64417-34-1 5-(N-Carbethoxy-N-methylaminoethyl)-5-(3-methoxyphenyl)-cyclopent-2-enon 
• 342405-60-1 2-(3-Methoxyphenyl)-2-(2-dimethylaminoethyl)-cyclopentanon 
• 61321-35-5 2-(3-Dimethylaminopropyl)-2-(3-methoxyphenyl)cyclopentanon 
• 288591-15-1 {(2R,6S)-6-[3-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-tetrahydro-pyran-2-yl}-acetic acid methyl ester 
• 288591-14-0 (E)-(S)-7-[3-(tert-Butyl-dimethyl-silanyloxy)-phenyl]-7-hydroxy-hept-2-enoic acid methyl ester 
• 288591-02-6 7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester 
• 288591-03-7 7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-hydroxy-hept-2-enoic acid methyl ester 
• 288591-01-5 5-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-5-oxo-pentanal 

Relevant academic research and scientific papers

Nickel-catalyzed Heck reaction of cycloalkenes using aryl sulfonates and pivalates

Nickel-catalyzed Heck reaction of cycloalkenes delivers unusual conjugated arylated isomers. Nickel(0) catalysts ligated by chelating dialkylphosphines effectively activate not only aryl triflates as electrophiles, but also less reactive aryl mesylates, t

Regio- and enantioselective Baeyer-Villiger oxidation: Kinetic resolution of racemic 2-substituted cyclopentanones

A kinetic resolution of racemic 2-substituted cyclopentanones via highly regio- and enantioselective Baeyer-Villiger oxidation has been successfully developed. The reaction could afford the normal 6-substituted δ-lactones in up to 98% ee and >19/1 regioselectivity. Meanwhile, the unreacted ketones were recovered in excellent ee values (up to 98%). It represents the best results of the kinetic resolution of racemic 2-substituted cyclopentanones via nonenzymic asymmetric BV oxidation.

Arenediazonium o-benzenedisulfonimides as efficient reagents for Heck-type arylation reactions

Arenediazonium o-benzenedisulfonimides can be used as new and efficient reagents for Heck-type arylation reactions of some common substrates containing C-C multiple bonds, namely ethyl acrylate, acrylic acid, acroleyne, styrene and cyclopentene. The reactions were carried out in an organic solvent, in the presence of Pd(OAc)2 as pre-catalyst, and gave rise to arylated products, for example, ethyl cinnamates, cinnamic acids, cinnamic aldehydes and stilbenes, possessing an (E)-configuration, and 1-arylcyclopentenes, in good to excellent yields. It is noteworthy that all the reactions led to the recovery, in greater than 80% yield, of o-benzenedisulfonimide, recyclable for the preparation of other diazonium salts.

Synthesis of simplified herboxidiene aromatic hybrids

The syntheses of simplified aromatic hybrids of the novel polyketide herboxidiene (1) are described. One of the hybrids prepared showed significant herbicidal activity against broad-leaved weeds in post-emergent application. (C) 2000 Elsevier Science Ltd. All rights reserved.

Synthesis and pharmacological activity of 6-aryl-2-azabicyclo[4.2.1]nonanes

A series of 6-phenyl-, 6-(m-methoxyphenyl)- and 6-(m-hydroxyphenyl)-2-azabicylo[4.2.1]nonanes was synthesized by a sequence involving alkylation of an appropriate 2-arylcyclopentanone with an aminoalkyl substituent. Subsequent ring closure at the other α