Mensen blijven massaal in Nederland vanwege corona | Omroep Brabant

Vakantie in eigen land was misschien nog nooit zo populair als nu. Mensen blijven massaal in Nederland vanwege de coronacrisis. De campings en vakantieparken in Brabant zitten goed vol nu de zomervakantie is begonnen. Maar hoe vier je nu vakantie in coronatijd én hoogseizoen? Al het Brabantse nieuws volgen? Abonneer je dan op ons kanaal: http://bit.ly/11jJQQT.

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11 Comments on “Mensen blijven massaal in Nederland vanwege corona | Omroep Brabant”

  1. Mensen zijn flink bang gemaakt, genoeg zodat ze hun verstand en individuele vrijheden hebben ingeleverd, voor slechts het illusie van wat veiligheid.
    Eerst was het hoe dodelijk de virus zou zijn, dan is het om IC capaciteit, het heeft allemaal reuze mee gevallen en nu ineens moeten mensen allemaal bang voor "besmettingen" zijn.
    Ook zonder de context dat 98% van de besmette gevallen er amper tot niets van merken, het is een loze angst. Waarom gebeurd dit allemaal?

  2. Aantal dingen zijn helaas goed voorspeld. Ik heb dit geschreven eind maart. Copy paste wordt gewaardeerd. Stay safe.
    C O R O N A – P L A N

    – Censuur op alle MSM kanalen (‘anders denkend’ deleted/banned)
    
- Money printer goes brrrr = € en $ devaluen
    
- Cashless society (door corona, cash = trash)

    – Cryptocurrency verboden per wet (terwijl dit juist de oplossing is, vanwege de decentralisatie en geen centrale bank die een bepaalde agenda heeft) 
Op moment van schrijven: false-flag ‘bitcoin hacks’ om crypto een slechte naam te geven en angst te zaaien

    – Tweede golf corona: masks worden verplicht, 1.5m in de grondwet (geen gezichtsuitdrukking, lachen, knuffelen, while those strengthen immune system)

    – Digitale overheidsmunt (“download de app en krijg €10.000 cadeau)
    
- Verplichte vaccinatie, anders outcast met geen rechten, bv reizen
    
- App en chip in de vaccinatie trackt alles wat je doet (USA en China = 1 camera per 4 ppl)
    

D O E L = One Global Government (centralised control)

  3. Ik las de componenten binnen de vaccin dat ze willen verspreiden Remdesivir is ook ineffectief was nutteloos met SARS en zelf simpele influenza ziektes. Erger nog er zitten explosieve materialen in deze vaccin die dood gevaarlijk zijn voor mensen. Deze vaccin en de test moet verboden worden voor deze redenen dat ze het nog steeds promoten is omdat mensen met heel veel geld en die willen nog meer geld verdienen tegelijkertijd de mensheid massa vermoorden spenderen heel veel geld om mensen te overtuigen. Dit is corruptie, verraad en massa moord. De vaccin was toch nutteloos tegen SARS en de Chinese griep is SARS-Cov 19. Ze gaan gewoon explosieve in je spuiten. Wie is dom genoeg om dit te accepteren??? Hell Gates wil de mensheid verminderen tot 500 million. mensen wereldwijd. Hoe denk je dat ie dat wil bereiken en wil ook nog eens dat jij betaald voor je eigen vernietiging en die van je familie.

    Synthesis of remdesivir in structural formulae

    Remdesivir can be synthesized in multiple steps from ribose derivatives. The figure to the right is one of the synthesis routes of remdesivir invented by Chun and coauthors from Gilead Sciences.[110][111] In this method, intermediate a is firstly prepared from L-alanine and phenyl phosphorodichloridate in presence of triethylamine and dichloromethane; triple benzyl-protected ribose is oxidized by dimethyl sulfoxide with acetic anhydride and give the lactone intermediate b; pyrrolo[2,1-f] [1,2,4]triazin-4-amine is brominated, and the amine group is protected by excess trimethylsilyl chloride. n-Butyllithium undergoes a halogen-lithium exchange reaction with the bromide at −78 °C (−108 °F) to yield the intermediate c. The intermediate b is then added to a solution containing intermediate c dropwise. After quenching the reaction in a weakly acidic aqueous solution, a mixture of 1: 1 anomers was obtained. It was then reacted with an excess of trimethylsilyl cyanide in dichloromethane at −78 °C (−108 °F) for 10 minutes. Trimethylsilyl triflate was added and reacts for one additional hour, and the mixture was quenched in an aqueous sodium hydrogen carbonate. A nitrile intermediate was obtained. The protective group, benzyl, was then removed with boron trichloride in dichloromethane at −20 °C (−4 °F). The excess of boron trichloride was quenched in a mixture of potassium carbonate and methanol. A benzyl-free intermediate was obtained. The isomers were then separated via reversed-phase HPLC. The optically pure compound and intermediate a are reacted with trimethyl phosphate and methylimidazole to obtain a diastereomer mixture of remdesivir. In the end, optically pure remdesivir can be obtained through chiral resolution methods.[citation needed]

    Dichloromethane (DCM or methylene chloride) is an organochloride compound with the formula CH2Cl2. This colorless, volatile liquid with a moderately sweet aroma is widely used as a solvent. Although >>>>>it is not miscible with water<<<<, it is polar, and miscible with many organic solvents.[11]

    Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH3)2SO. This colorless liquid is an important polar aprotic solvent that dissolves both polar and nonpolar compounds and is miscible in a wide range of organic solvents as well as water. It has a relatively high boiling point. DMSO has the unusual property that many individuals perceive a garlic-like taste in the mouth after contact with the skin.[3]
    In terms of chemical structure, the molecule has idealized Cs symmetry. It has a trigonal pyramidal molecular geometry consistent with other three-coordinate S(IV) compounds,[4] with a nonbonded electron pair on the approximately tetrahedral sulfur atom.

    Trimethylsilyl chloride, also known as chlorotrimethylsilane is an organosilicon compound (silyl halide), with the formula (CH3)3SiCl, often abbreviated Me3SiCl or TMSCl. It is a colourless volatile liquid that is stable in the absence of water. It is widely used in organic chemistry.

    n-Butyllithium (abbreviated n-BuLi) is an organolithium reagent. It is widely used as a polymerization initiator in the production of elastomers such as polybutadiene or styrene-butadiene-styrene (SBS). Also, it is broadly employed as a strong base (superbase) in the synthesis of organic compounds as in the pharmaceutical industry.

    Butyllithium is commercially available as solutions (15%, 25%,1.5 M, 2 M, 2.5 M, 10 M, etc.) in alkanes such as pentane, hexanes, and heptanes. Solutions in diethyl ether and THF can be prepared, but are not stable enough for storage. Annual worldwide production and consumption of butyllithium and other organolithium compounds is estimated at 2000 to 3000 tonnes.[2]

    Organolithium reagents are organometallic compounds that contain carbon – lithium bonds. They are important reagents in organic synthesis, and are frequently used to transfer the organic group or the lithium atom to the substrates in synthetic steps, through nucleophilic addition or simple deprotonation.[1] Organolithium reagents are used in industry as an initiator for anionic polymerization, which leads to the production of various elastomers. They have also been applied in asymmetric synthesis in the pharmaceutical industry.[2] Due to the large difference in electronegativity between the carbon atom and the lithium atom, the C-Li bond is highly ionic. Owing to the polar nature of the C-Li bond, organolithium reagents are good nucleophiles and strong bases. For laboratory organic synthesis, many organolithium reagents are commercially available in solution form. These reagents are highly reactive, and are sometimes pyrophoric.

    Je wordt een lopende bomb letterlijk.

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