54988-93-1

Upstream product

• 186581-53-3 diazomethane 
• 54988-91-9 5-phenylbenzanthracene-7,12-dione 
• 26037-61-6 2-bromo-3-methoxy-1,4-naphthoquinone 
• 201416-09-3 C₁₂H₉BrO₃ 
• 1211483-19-0 methyl 4-bromo-3-methoxy-2-naphthoate 
• 1246811-81-3 methyl 3-methoxy-4-phenyl-2-naphthoate 
• 13041-60-6 methyl 3-methoxy-2-naphthoate 
• 135-19-3 β-naphthol 
• 92-70-6 3-Hydroxy-2-naphthoic acid 
• 83303-57-5 methyl 1,2-dihydro-1-phenylnaphthalene-3-carboxylate 

Relevant academic research and scientific papers

Allylic Phosphorus Ylides Directly Generated from Alcohols with Water as the only Byproduct

A novel strategy for the preparation of allylic phosphorus ylides directly from Morita-Baylis-Hillman (MBH) alcohols in an environmentally benign manner was developed. With the assistance of a calcium catalyst, the SN2′ process between phosphin

The Baylis-Hillman acetates in organic synthesis: Unprecedented sodium nitrite induced intramolecular Friedel-Crafts cyclization of secondary nitro compounds

Unprecedented sodium nitrite mediated intramolecular Friedel-Crafts cyclization of alkyl (E)-2-arylidene-4-nitroalkanoates and (E)-3-arylidene-5- nitroalkan-2-ones derived from Baylis-Hillman acetates, providing a facile protocol for synthesis of naphthal

2,3-Dichloro-5,6-dicyano-para-benzoquinone (DDQ)/methanesulfonic acid (MsOH)-mediated intramolecular arene-alkene oxidative coupling

An efficient intramolecular arene-alkene oxidative coupling of 1,4-diaryl-1,3-butadienes has been developed involving the use of a 2,3-dichloro-5,6-dicyano-para-benzoquinone (DDQ)/acid catalyst. The reaction involves the generation of a radical cation by abstraction of an electron from the substrate with DDQ, an intramolecular Friedel-Crafts-type reaction, and the loss of hydrogen radical.

Ni-catalyzed reduction of inert C-O bonds: A new strategy for using aryl ethers as easily removable directing groups

An efficient Ni-catalyzed protocol for the reductive cleavage of inert C-O bonds has been developed. The method is characterized by its simplicity and wide scope, thereby allowing the use of aryl ethers as easily removable directing groups in organic synthesis.