Chemistry graduates have much scope to use their knowledge in a range of research sectors, including roles within chemical engineering, chemical and related industries, healthcare and more. Recommanded Product: 56786-63-156786-63-1, Name is (2AR,2’R,4S,5’R,6aR,6bS,8aS,8bR,9S,11aS,12aS,12bS)-2a,4-dihydroxy-5′,6a,8a,9-tetramethylicosahydrospiro[naphtho[2′,1′:4,5]indeno[2,1-b]furan-10,2′-pyran]-2(11aH)-one, SMILES is [H][C@]1(O[C@@]2(OC[C@H](C)CC2)[C@H]3C)C[C@@]4([H])[C@]5([H])CC([C@@]6(O)C[C@@H](O)CC[C@]6(C)[C@@]5([H])CC[C@]4(C)[C@]13[H])=O, belongs to dioxole compound. In a article, author is Aitken, R. Alan, introduce new discover of the category.
The most important new developments in the chemistry of 1,3-dioxole- and 1,3-oxathiole-based ring systems over the period 2007-2012 are described in four major sections with 200 literature references. Properties such as theoretical and experimental structure determination are discussed including X-ray structure determination and nuclear magnetic resonance studies. Reactivity is considered in the categories of nucleophilic attack at ring carbon atoms, ring deprotonation, radical and carbene reactions and halogenation, and reactivity at ring substituents. Synthesis is covered in detail with new methods categorized according to the number of ring bonds formed and the fragments involved. Finally, applications are described for individual compounds in areas such as polymers, electronics, batteries, chiral NMR shift reagents, chiral catalysts, chiral ligands, and pharmaceuticals.
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Reference:
1,3-Benzodioxole – Wikipedia,
,Dioxole | C3H4O2 – PubChem