111170-32-2

Upstream product

• 111170-31-1 3-(2-Benzenesulfonylmethyl-phenyl)-propionic acid methyl ester 
• 88116-02-3 1-bromomethyl-2-[(phenylsulfonyl)methyl]benzene 
• 108-59-8 malonic acid dimethyl ester 

Downstream Products

• 111170-33-3 2-[3-(2-Benzenesulfonylmethyl-phenyl)-propyl]-malonic acid dimethyl ester 
• 113811-90-8 Methanesulfonic acid 3-(2-benzenesulfonylmethyl-phenyl)-propyl ester 
• 113812-10-5 1-Benzenesulfonylmethyl-2-(3-iodo-propyl)-benzene 
• 113830-93-6 1-(4-hydroxy-1-butyl)-2-<(phenylsulfonyl)methyl>benzene 
• 113811-98-6 1-(3-cyano-1-propyl)-2-<(phenylsulfonyl)methyl>benzene 
• 113812-01-4 2,3,3a,4,5,9b-hexahydro-4-oxo-5-(phenylsulfonyl)benzindene 
• 113811-91-9 2-<3-<2-<(phenylsulfonyl)methyl>phenyl>propyl>cyclopentanone 
• 113811-99-7 1-<5,5-bis(methoxycarbonyl)-1-pentyl>-2-<(phenylsulfonyl)methyl>benzene 
• 113811-96-4 (6R,8R)-6-Benzenesulfonyl-7-oxo-6,7,9,11,12,13,14,15,16,17-decahydro-cyclopenta[a]phenanthrene-8-carboxylic acid methyl ester 
• 113812-00-3 2-[4-(2-Benzenesulfonylmethyl-phenyl)-4-bromo-butyl]-malonic acid dimethyl ester 
• 113811-93-1 2-{2-[3-(2-Benzenesulfonylmethyl-phenyl)-propyl]-cyclopentyl}-malonic acid dimethyl ester 
• 113811-95-3 2-{2-[3-(2-Benzenesulfonylmethyl-phenyl)-3-bromo-propyl]-cyclopentyl}-malonic acid dimethyl ester 
• 113811-92-0 2-{2-[3-(2-Benzenesulfonylmethyl-phenyl)-propyl]-cyclopentylidene}-malonic acid dimethyl ester 
• 111170-29-7 2-[3-(2-Benzenesulfonylmethyl-phenyl)-3-bromo-propyl]-malonic acid dimethyl ester 

Relevant academic research and scientific papers

New Syntheses of Phenanthrenes and of Related Systems by Intramolecular Annulation Processes

A regio- and stereoselective intramolecular double annulation, which converts monocyclic aromatic compounds into partly reduced phenanthrenes, is described.Methoxy- (9a,c) and benzene derivatives (9b) with a (5-bromoalkyl)mal

SYNTHESIS AND CHEMICAL TRANSFORMATIONS OF CYCLOBUTANAPHTHALENE AND -ANTHRACENE DERIVATIVES

Cyclobutanaphthalene derivatives (2a-c) and an anthracene analog (2d) were prepared by a double annulation procedure from mono- and bicyclic precursors (1a-d).Compound 2a was further converted to 3-hydroxynaphtocyclobutene (10), to the novel quinone