Top 10 similar words or synonyms for naoac

trishcl    0.782487

naacetate    0.752509

naac    0.747082

triscl    0.729674

nacitrate    0.708297

mgac    0.704047

guscn    0.699614

koac    0.698662

teaa    0.687098

oac    0.683817

Top 30 analogous words or synonyms for naoac

Article Example
Sodium acetate Sodium acetate, CHCOONa, also abbreviated NaOAc, also known as sodium ethanoate, is the sodium salt of acetic acid. This colorless deliquescent salt has a wide range of uses.
Larock indole synthesis Monguchi et al. also derived 2- and 2,3-substituted indoles without using LiCl. The optimized Indole reaction uses 10% Pd/C (3.0 mol%) with 1.1 equivalent of NaOAc, and NMP at 110–130 °C. Monguchi et al. state that their optimized condition of the Larock indole synthesis without LiCl is a more mild, environmentally benign, and efficient strategy for producing indoles.
Magnesium acetate Magnesium acetate has been found to cause a conformational change in "Escherichia coli" enzyme Primase. In this experiment Mg(OAc), MnCl, CaCl, NaOAc, LiCl, MgSO and MgCl were all compared to see what effect they had on the "Escherichia coli" enzyme Primase. The experimenters found that Mg(OAc) caused the best conformational change. MgSO and MgCl induced the effect slightly while the rest did not.
Acetate When part of a salt, the formula of the acetate ion is written as CHCO, CHO, or CHCOO. Chemists abbreviate acetate as OAc or, less commonly, AcO. Thus, HOAc is the abbreviation for acetic acid, NaOAc for sodium acetate, and EtOAc for ethyl acetate. The abbreviation "Ac" (or "AC") is also sometimes encountered in chemical formulas to indicate the acetate ion (CHCO), or the acetyl group (CHCO). This abbreviation is not to be confused with the symbol of actinium, the first element of the actinide series. For example, the formula for sodium acetate might be abbreviated as "NaAc", rather than "NaCHO". Care should also be taken to avoid confusion with peracetic acid when using the OAc abbreviation; for clarity and to avoid errors when translated, HOAc should be avoided in literature mentioning both compounds.
Takahashi Taxol total synthesis Cyclisation of 27 took place by alkylation (LiN(TMS), dioxane, microwave irradiation) to tricycle 28. Subsequent steps were cyanohydrin hydrolysis (camphorsulfonic acid), TMS deprotection (KOH) and allylic oxidation (SeO, tBuOH, salicylic acid) to ketone 29, then Upjohn dihydroxylation to triol 30, then acylation (AcCl, DMAP) and mesitylation (MsCl, DMAP) to 31, then benzyl group and benzyloxy group removal (hydrogenation / Palladium on carbon) followed by carbonate protection (triphosgene, pyridine) to 32, then secondary alcohol protection (TESCl, pyridine) and primary alcohol deprotection (potassium carbonate) to diol 33, then oxetane formation (DIPEA, HMPA) to 34, then acylation (AcO, DMAP), then benzoylation (phenyllithium) to 35, then oxidation (tBuOK, (PhSeO)O, THF) to the acyloin 36, then isomerisation (tBuOK) and acylation (AcO, DMAP, pyr) to 37, then oxidation at the allylic position (PCC, celite, NaOAc, benzene), ketone group oxidation (NaBH) and TES protecting group removal (HF·pyr) to baccatin III (38).