RNA molecules have various applications in living cells, such as 1) transmission and translation of genetic information, 2) structural support of molecular machines, 3) regulation of gene expression, silencing and catalysis. Obtaining a complete spatiotemporal distribution of RNA synthesis, processing, and transportation is essential for understanding the function and behavior...

By Qinling Li Read more

The Wolff-Kishner reduction uses hydrazine, a base, and a high-boiling solvent to convert an aldehyde or ketone to an alkane. The hydrazine first attacks the ketone or aldehyde, releasing water to form a hydrazone intermediate. Subsequent proton transfer steps result in the release of nitrogen gas and the formation of...

By shuhan yang Read more

The Wolff rearrangement uses either catalytic silver oxide, heat, or light to convert an α-diazo ketone to a ketene. In a one-step reaction, the catalyst initiates a 1,2-shift to release nitrogen gas and produce ketene. Due to the release of nitrogen gas, this reaction should not be performed in a...

By shuhan yang Read more

Repurposed from a prokaryotic adaptive immune response, the CRISPR/Cas9 system has become a powerful RNA-guided genome-editing tool for targeting and manipulating virtually any genomic sequence, since its inception in 2012.  Nowadays CRISPR is being used in a plethora of applications including the elucidation of gene function involved in disease, the...

By shuhan yang Read more

The Wurtz coupling uses sodium metal and two alkyl halides to make a new carbon-carbon bond. First, a metal-halogen exchange forms a carbanion that then attacks the second alkyl halide in SN2 fashion. Reagents: Sodium Metal, Solvent (THF, Et2O, Dioxane, Xylenes) Reactant: Alkyl Halide Product: Alkane Type of Reaction: Metal-Catalyzed...

By shuhan yang Read more

The Yamaguchi esterification converts a carboxylic acid to an ester. First, triethylamine (Et3N) deprotonates the carboxylic acid, which then attacks the Yamaguchi reagent (2,4,6-trichlorobenzoyl chloride) to produce an acid anhydride. The Yamaguchi reagent is released when the acid anhydride is attacked by 4-dimethylaminopyridine (DMAP). The alcohol displaces DMAP and a...

By shuhan yang Read more
Just added to your wishlist:
My Wishlist
You've just added this product to the cart:
Go to cart page