Reactions of photoexcited SO2; preparation of α-substituted alkanesulphinic acids
✍ Scribed by J.R. Nooi; P.C. van der Hoeven; W.P. Haslinghuis
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 153 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Irradiation of SOe in the gas phase with W-light in the presence of gaseous alkahes leads to the formation of alkanesulphinic acids (1). When SOe is irradiated in the presence of cis-or trans-butene, cis/trahs isomerization occurs (21, whilst in the presence of biacetyl, phosphorescence from biacetyl is observed (3). Photolysis of SOs within the first allowed absorption band leads to SOs (4). These reactions are assumed to proceed via excited SOs (2-5). The initiation of the liquid-phase reaction (6,7) between alkanes, SOs and Oa (sulphoxidation, leading to alkanesulphonic acids) is also supposed to proceed via excited SOs (8,9). Here we present another * When a mixture of a solution Xf 2-propanol and SO, (0.55 and 0.37 molar respectively) in Ccl, was irradiated at +20 C, acetone was formed in a yield of 31 mole% in 6 h. However, also water, sulphur, chloroform and Cl-ions were formed, the latter two indicating that Ccl, is taking part in the reaction ( 14).
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## Abstract For Abstract see ChemInform Abstract in Full Text.
N-1-(Carbamate protected)-N-2-(alkyl or aryl substituted) hydrazines can serve as amine substrates for the Petasis boronic acid-Mannich reaction, providing a practical synthetic route for the preparation of a-hydrazinocarboxylic acids. The scope and limitations of this method have been examined.