188824-19-3

Upstream product

• 3040-44-6 1-piperidinoethanol 
• 188824-63-7 2,8-dimethoxy-5-[4-[(tert-butyldimethylsilyl)oxy]phenyl]-11,12-dihydro-6H-benzo[c]phenanthrid-6-one 
• 188824-62-6 6-methoxy-1-[N-[[4-(tert-butyldimethylsilyl)oxy]phenyl]-N-(2,5-dimethoxybenzoyl)]amino-3,4-dihydronaphthalene 
• 188824-64-8 2,8-dimethoxy-5-[4-hydroxyphenyl]-11,12-dihydro-6H-benzo[c]phenanthrid-6-one 
• 188824-61-5 [4-(tert-butyl-dimethyl-silanyloxy)-phenyl]-(6-methoxy-3,4-dihydro-2H-naphthalen-1-ylidene)-amine 
• 188824-60-4 6-methoxy-1-[(4-hydroxy)phenyl]imino-1,2,3,4-tetrahydronaphthalene 
• 123-30-8 4-amino-phenol 
• 17918-14-8 2,5-dimethoxybenzoyl chloride 
• 188824-23-9 2,8-dimethoxy-5-[4-[2-(1-piperidinyl)ethoxy]phenyl]-11,12-dihydro-6H-benzo[c]phenanthrid-6-one 

Relevant academic research and scientific papers

Photochemical synthesis of N-arylbenzophenanthridine selective estrogen receptor modulators (SERMs)

Selective estrogen receptor modulators are an emerging class of pharmaceutically important molecules. Many compounds in this class contain an aminoethoxyaryl moiety attached to a polycyclic framework at an asymmetric carbon atom. To assess whether this ca

Pentacyclic compounds, intermediates, processes, compositions, and methods

The present invention provides compounds of formula I: STR1 wherein X is --O-- or --S--, Y is --O--, --S--, --CH2 --, --CH2 CH2 --, --CH=CH--, or --NR5 --; R1, R2, and R3 are eac

Pentacyclic compounds, intermediates, processes, compositions, and methods

The present invention relates to compounds of formula I and II; wherein X is -O-, -S-, or -NR5-; Y is -O-, -S-, -CH2-, -CH2CH2-, -CH=CH-, or -NR5-; B is -CH2- or -CO-; R1, R