Results 61 to 70 of about 9,174 (269)

Naphthalenes in Cigarette Smoke [PDF]

open access: yesNature, 1963
IN our work on the composition of the non-methanol volatile neutral fraction of cigarette smoke we have isolated and identified the naphthalenes shown in Table 1.
R A, JOHNSTONE, P M, QUAN
openaire   +2 more sources

Optimized Lipid Nanoparticles with Tail‐Modified Ionizable Lipids for Safer mRNA Delivery

open access: yesAdvanced Science, EarlyView.
Systematic engineering of hydrophobic tail architecture in vitamin B5‐derived ionizable lipids establishes a comprehensive structure–activity relationship framework for mRNA delivery. Combined lipidtail and formulation optimization identifies TM1‐OPT3‐C, a lipid nanoparticle platform that improves efficacy–safety balance through efficient mRNA delivery,
Seo‐Hyeon Bae   +27 more
wiley   +1 more source

Oxidation of Alkylaromatics

open access: yesE-Journal of Chemistry, 2007
Hydroperoxide at α-position to the aromatic ring is the primary oxidation product formed. In all cases monoalkylbenzenes lead to the formation of benzoic acid.
T. S. S. Rao, Shubhra Awasthi
doaj   +1 more source

Synthesis and Host–Guest Properties of Acyclic Pillar[n]naphthalenes

open access: yesFrontiers in Chemistry, 2019
Here we report a new class of synthetic receptors, acyclic pillar[n]naphthalene (n = 2–4, Dimer, Trimer, and Tetramer) oligomers, which are made up of 2,3-diethoxynaphthalene units linked by methylene bridges at the 1- and 4-positions.
Yuanyin Jia   +5 more
doaj   +1 more source

A Modular Standard Operating Procedure for Standardizing Lithium Metal Interfaces

open access: yesAdvanced Science, EarlyView.
A modular standard operating procedure (SOP) is developed to standardize lithium metal interfaces through sequential etching, brushing, and soaking. By transforming poorly controlled lithium surfaces into chemically uniform and structurally regulated interfaces, the framework improves electrochemical reproducibility, interfacial stability, and ...
Wen‐Hsin Chang   +7 more
wiley   +1 more source

Naphthalene plasmids in pseudomonads [PDF]

open access: yesJournal of Bacteriology, 1982
A rapid method beginning with the direct lysis of bacteria in alkaline sodium dodecyl sulfate was used to detect naphthalene plasmids in pseudomonads. The strains NCIB 9816, PG, ATCC 17483, and ATCC 17484, which can grow on naphthalene as the sole source of carbon and energy, were examined. All except ATCC 17483 contained more than one plasmid.
M A, Connors, E A, Barnsley
openaire   +2 more sources

Metal triflate promoted synthesis of naphthalenes

open access: yes, 2017
A synthetic route to derive the skeleton of naphthalenes starting with isovanillin is described with modest total yieldsviathe key transformation of metal triflate-mediated intramolecular benzannulation ofo-formyl oro-benzoyl allylbenzenes in MeNO2at rt.
Yu-Lin Tsai   +3 more
core   +1 more source

N–O Dual Functional Group Transposition via Energy Transfer Photocatalysis

open access: yesAdvanced Science, EarlyView.
N–O dual functional group transposition (dFGT) enabled by the photocatalytic energy transfer (EnT) has been developed. This methodology is applicable to both activated and unactivated alkyl derivatives for dFGT, and it also successfully extended to N–N dFGT, demonstrating its general applicability.
Lei Bao   +4 more
wiley   +1 more source

Beyond Traditional Phenolics: Disulfide Bonds for Performance Enhancement of Aerospace Ablation‐Resistant Materials from Processing to Recycling

open access: yesAdvanced Science, EarlyView.
The dynamic disulfide bonds facilitated the development of high‐performance aerospace ablation‐resistant materials. At moderate temperature, the dissociation and recombination of disulfide bonds ensured excellent processability, mechanical properties, and recycling ability of phenolic resin; at high temperature, cleavage of disulfide bonds produced ...
Yu Li   +9 more
wiley   +1 more source

One‐Pot Ruthenium‐Catalyzed Synthesis of Benzyl/Allyl‐Halide Substituted (dihydro)naphthalenes via Radical Benzannulation

open access: yesChemistryEurope
Herein, a selective, one‐pot synthetic route to reactive benzyl‐ and allyl‐halide‐substituted naphthalenes and dihydronaphthalenes from easily accessible 2,3‐aryl‐1,3‐butadiene substrates and simple halogenated alkanes, using [Cp*RuCl(PPh3)2] as the ...
Nicole S. van Leeuwen   +9 more
doaj   +1 more source

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