13523-64-3

Upstream product

• 110391-94-1 4-ethyl-4-methoxycyclohexa- 2,5-dien-1-one 
• 112824-28-9 2-ethyl-4-t-butyldimethylsiloxyphenol 
• 2349-70-4 2-ethylhydroquinone 
• 103323-26-8 3-ethyl-4-methoxy-benzaldehyde 

Downstream Products

• 95227-10-4 N-Acetyl-3-<3,5-dinitro-4-(4-methoxy-3-ethyl-phenoxy)-phenyl>-DL-2-amino-propionsaeure-ethylester 
• 95227-10-4 L-N-Acetyl-3-<3,5-dinitro-4-(4-methoxy-3-ethyl-phenoxy)-phenyl>-2-amino-propionsaeure-ethylester 
• 914775-95-4 2-tert-butyl-5-ethyl-4-methoxy-phenol 
• 95133-14-5 DL-N-Acetyl-3-<3,5-diiod-4-(4-methoxy-3-ethyl-phenoxy)-phenyl>-2-amino-propionsaeure-ethylester 
• 3458-13-7 DL-3,5-Diiod-3'-ethyl-thyronin 

Relevant academic research and scientific papers

Re2O7 catalyzed dienone-phenol rearrangement

The dienone-phenol rearrangement of 4,4-disubstituted cyclohexadienones catalyzed by Re2O7 has been described. Multi-substituted phenols can be efficiently obtained in good to excellent yields by employing this catalytic protocol.

Synthesis and biological activity of phenoxyphenyl oxamic acid derivatives related to L-Thyronine

The synthesis of substituted phenoxyphenyl oxamic acid derivatives related to L-thyronine (L-T3) is described. The in vitro and in vivo cholesterol lowering and cardiovascular effects of these compounds are presented and discussed. (C) 2000 Elsevier Science Ltd. All rights reserved.