Simple exploration of 63-37-6

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 63-37-6. Quality Control of 5′-Cytidylic acid.

Chemistry, like all the natural sciences, Quality Control of 5′-Cytidylic acid, begins with the direct observation of nature¡ª in this case, of matter.63-37-6, Name is 5′-Cytidylic acid, SMILES is O=P(O)(OC[C@@H]1[C@H]([C@H]([C@H](N2C(N=C(C=C2)N)=O)O1)O)O)O, belongs to benzodioxans compound. In a document, author is WELL, M, introduce the new discover.

SYNTHESIS AND NMR-SPECTROSCOPY OF PHOSPHORANES WITH 1,3,2-DIOXA-4,5-NAPHTHOPHOSPHOLE RING

The reaction of naphthalene-2,3-diol 1 with PCl3 was found to furnish the hydridophosphorane 3, with PCl5 the chlorophosphorane 4 was formed. The reaction of the fluorophosphoranes, RPF4 [R=F, (i)Pr, CH2SiMe3, CH2Cl, Ph] with the bis(trimethylsilyl) derivative of 1, 2 yielded the corresponding spirocyclic phosphoranes, 5-9 by cleavage of the Si-O bond and elimination of Me3SiF. The difluorophosphoranes, R2PF3 [R=Me, Ph] reacted with 2 to form the monocyclic phosphoranes, 10 and 11, where the fluorine atom occupies an axial position at trigonal-bipyramidal (TBP) phosphorus- The structure of compound 11 was confirmed by single crystal X-ray analysis of its dichloromethane hemisolvate at -95-degrees-C. The geometry at phosphorus is trigonal-bipyramidal. whereby the naphthalenedioxy ligand spans an axial and an equatorial site. Me2PF3 reacted with tetrakis(1,2,4.5-trimethylsiloxy)benzene to form the bifunctional benzodioxa-lambda5-phosphole, 12.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 63-37-6. Quality Control of 5′-Cytidylic acid.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem