65755-81-9

Upstream product

• 60168-64-1 1-phenyl-2-(2-propenyloxy)-1-ethanol 
• 582-24-1 1-phenyl-2-hydroxyethanone 
• 106-95-6 allyl bromide 
• 51336-63-1 (allyloxy)acetonitrile 

Downstream Products

• 65755-91-1 2-phenyl-2-(trimethylsiloxy)-4-pentenal 
• 98015-24-8 2-(allyloxy)-1-phenylpropan-1-one 
• 1215085-65-6 5-phenyl-5-(2-propenyloxy)methylimidazolidine-2,4-dione 
• 1333391-85-7 2-allyl-6-chloro-2-phenylindolin-3-one 
• 6249-80-5 1-phenylbut-3-en-1-one 
• 87258-91-1 3-hydroxy-3-phenylhex-5-en-2-one 
• 123507-41-5 2-Hydroxy-2-methyl-1-phenyl-pent-4-en-1-one 
• 123507-26-6 N'-[2-Allyloxy-1-phenyl-eth-(E)-ylidene]-N,N-dimethyl-hydrazine 
• 7782-21-0 (RS)-2-phenylpentanoic acid 

Relevant academic research and scientific papers

Facile access to 2,2-disubstituted indolin-3-ones: Via a cascade Fischer indolization/Claisen rearrangement reaction

An efficient approach for the synthesis of 2,2-disubstituted indolin-3-ones is described. From readily accessible aryl hydrazines and allyloxyketones, 2,2-disubstituted indolin-3-ones could be obtained in good to excellent yields under mild reaction condi

Catalytic ketyl-olefin cyclizations enabled by proton-coupled electron transfer

Concerted proton-coupled electron transfer is a key mechanism of substrate activation in biological redox catalysis. However, its applications in organic synthesis remain largely unexplored. Herein, we report the development of a new catalytic protocol fo

Identification of a 4-(hydroxymethyl)diarylhydantoin as a selective androgen receptor modulator

Structural modification performed on a 4-methyl-4-(4-hydroxyphenyl) hydantoin series is described which resulted in the development of a new series of 4-(hydroxymethyl)diarylhydantoin analogues as potent, partial agonists of the human androgen receptor. T

NOVEL IMIDAZOLIDINE COMPOUNDS AS ANDROGEN RECEPTOR MODULATORS

Novel compounds are disclosed that have a Formula represented by the following: wherein X, R1, R2a, R2b, R2c, R3a R3b, R4a, R4b, R4c, and ml are as describe

An alternative to the Swern oxidation

A variety of alcohols have been oxidized under mild conditions by the DMSO-Ph3P·X2 complexes. The reaction does not produce any Pummerer product. A mechanism for the reaction is proposed.