Results 131 to 140 of about 9,174 (269)

Infrared and ultraviolet spectrophotometric analysis of chromatographic fractions of crude oils and petroleum products

open access: yesBulletin of the Chemical Society of Ethiopia, 2007
Samples of light, medium and heavy Nigerian crude oils and petroleum products including diesel oil, engine oil (SAE 40) and gasoline (PMS) have been separated into four fractions of saturates, monoaromatics, diaromatics and polyaromatics by elution ...
E.O. Odebunmi, S.A. Adeniyi
doaj  

Regioselective Synthesis and Cytotoxic Effects of New Juglone Derivatives with an Aliphatic Substituent at C(2) or C(3)

open access: yesBiomolecules
The naphthoquinone juglone (5-hydroxynaphthalene-1,4-dione) (1) occurs abundantly in nature, especially in species belonging to the Juglandaceae family. Due to its multifaceted biological activities, this compound is considered a privileged structure in ...
Giovanni Vidari   +5 more
doaj   +1 more source

The metalation of 1- and 2-(trifluoromethyl)naphthalenes: Noteworthy site selectivities

open access: yes
This article provides insight into the various factors by which electroneg. substituents affect the kinetic acidity of arenes and, more specifically, naphthalenes.
Cottet, Fabrice   +2 more
core   +1 more source

Synthesis of Dihomocalix[4]naphthalenes:  First Members of a New Class of [1.2.1.2](1,3)Naphthalenophanes

open access: yes, 2016
Synthesis of Dihomocalix[4]naphthalenes:  First Members of a New Class of [1.2.1.2](1,3 ...
Paris E. Georghiou (828618)   +3 more
core   +1 more source

Water, Alcohols, Amines, and Amides as Formal Hydrogen‐Atom‐Transfer Reagents Through Activation With Redox‐Active Lewis Acids

open access: yesAngewandte Chemie, EarlyView.
Protic molecules containing strong O─H or N─H bonds typically resist hydrogen‐atom abstraction because of the high reactivity of the resulting heteroatom‐centered radicals. However, association of the protic molecules with redox‐active Lewis acids can provide powerful hydrogen‐atom donors or proton‐coupled‐electron‐transfer reagents.
Petra Vojáčková, Armido Studer
wiley   +2 more sources

Synthesis of Large‐ and Medium‐Sized Heterobiaryl Atropisomeric Rings and Atropopeptides by Catalytic Intramolecular SNAr

open access: yesAngewandte Chemie, EarlyView.
Catalytic, intramolecular N‐heterocycle arylation by nucleophilic aromatic substitution (SNAr) is now available for synthesis of highly strained macrocycles and medium‐sized heterobiaryl atropisomeric rings, including atropopeptides. Key to the approach is the ability to generate a strong base catalytically, taking advantage of base‐embedding ...
Alireza Abbasi Kejani   +7 more
wiley   +2 more sources

1,2‐Bis(boronate) Arenes by Borylation Directed Borylation

open access: yesAngewandte Chemie, EarlyView.
Boron electrophiles derived from tetrabromo‐pyrazaboles and AlCl3 affect the regioselective vicinal double C–H borylation of a range of arenes and polycyclic aromatic hydrocarbons (PAHs). A subsequent pinacol installation step then affords the vicinal bis‐boronate ester‐substituted arene/PAH.
Anna V. Schellbach   +4 more
wiley   +2 more sources

An X‑Shaped Chiral Non‑Fullerene n‐Type Semiconductor: Application in Perovskite Solar Cells and Chirality‑Induced Spin Selectivity

open access: yesAngewandte Chemie, EarlyView.
A highly electron‑accepting derivative of cyclobisbiphenylenecarbonyl (CBBC‐TIC) is reported. CBBC‐TIC functions as an electron‐transport layer for perovskite solar cells, achieving a power conversion efficiency of 20.6%. Furthermore, the enantiomers of CBBC‐TIC exhibited spin‐selective electron transport with high enantiospecific magnetic conductance ...
Yuki Sakamoto   +15 more
wiley   +2 more sources

Benzotriazole-Assisted Aromatic Ring Annulation:  Efficient and General Syntheses of Polysubstituted Naphthalenes and Phenanthrenes

open access: yes, 2016
(Benzotriazol-1-ylmethyl)benzenes and -naphthalenes 1a−f, easily accessible from benzyl bromides and benzotriazole, readily undergo lithiation and subsequent 1,4-addition to α,β-unsaturated aldehydes and ketones.
Linghong Xie (3037746)   +2 more
core   +1 more source

Phosphine-Mediated Multi-Component γ-Umpolung/Aldol/Wittig Cascade Reaction for the Synthesis of Functionalized Naphthalenes [PDF]

open access: yes, 2013
This study describes an efficient and convenient triphenylphosphine-mediated γ-umpolung/aldol/Wittig cascade reaction. This is the first time that phosphine has been used to mediate a multi-component coupling reaction involving alleonates, nucleophiles ...
Zhang, Kui
core  

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