Intramolecular Alkene–Alkene Coupling via Rh(III)-Catalyzed Alkenyl sp2 C–H Functionalization: Divergent Pathways to Indene or α-Naphthol Derivatives

ACS Catalysis ◽  
2021 ◽  
Vol 11 (18) ◽  
pp. 11494-11500
Author(s):  
Manikantha Maraswami ◽  
Thomas Diggins ◽  
Jeffrey Goh ◽  
Raymond Tio ◽  
Wan Qing Renee Ong ◽  
...  
Keyword(s):  
Naphthol Derivatives

ChemInform Abstract: Synthesis of New and Novel N-Protected 1-Aminoalkyl-2-naphthol Derivatives.

ChemInform ◽  
2009 ◽  
Vol 40 (50) ◽  
Author(s):  
Hamid Reza Shaterian ◽  
Asghar Hosseinian ◽  
Majid Ghashang
Keyword(s):  
Naphthol Derivatives

Synthesis of Novel 2-(2-Cyclopentyl)- and 2-(2-Cyclohexyl) Substituted 1-Naphthol Derivatives with Anticyclooxygenase Activity

2006 ◽  
Vol 13 (30) ◽  
pp. 3663-3674 ◽  
Author(s):  
Ngampong Kongkathip ◽  
Komkrit Hasitapan ◽  
Narathip Pradidphol ◽  
Kanyawim Kirtikara ◽  
Nipa Jongkon ◽  
...  
Keyword(s):  
Substituted 1 ◽  
Naphthol Derivatives

Asymmetric ring-opening of cyclopropyl ketones with β-naphthols catalyzed by a chiral N,N′-dioxide–scandium(iii) complex

2018 ◽  
Vol 5 (8) ◽  
pp. 1293-1296 ◽  
Author(s):  
Yong Xia ◽  
Fenzhen Chang ◽  
Lili Lin ◽  
Yali Xu ◽  
Xiaohua Liu ◽  
...  
Keyword(s):  
Ring Opening ◽  
Complex Catalyst ◽  
Ring Opening Reaction ◽  
Cyclopropyl Ketones ◽  
Naphthol Derivatives ◽  
Asymmetric Ring Opening ◽  
Asymmetric Ring Opening Reaction

An efficient asymmetric ring-opening reaction of cyclopropyl ketones with 2-naphthols has been realized using a chiral N,N′-dioxide–ScIII complex catalyst. A variety of chiral β-naphthol derivatives were obtained in excellent outcomes (up to 99% yield, 97% ee).

ChemInform Abstract: Aerobic Oxidative Coupling of 2-Naphthol Derivatives Catalyzed by a Copper-Amine Complex Without Solvent.

ChemInform ◽  
2010 ◽  
Vol 30 (21) ◽  
pp. no-no
Author(s):  
Makoto Nakajima ◽  
Shun-ichi Hashimoto ◽  
Masahiro Noji ◽  
Kenji Koga
Keyword(s):  
Oxidative Coupling ◽  
Amine Complex ◽  
Naphthol Derivatives ◽  
Copper Amine
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