## Abstract The photochemistry of the α‐diazo sulfoxide **7** has been investigated in solid argon at 10 K by IR spectroscopy. The sulfinyl carbene was not detected directly but instead underwent photochemically induced hetero‐Wolff rearrangement to the sulfine **8** which could be detected and cha
Stereoespecific syntheses of 2,3-dimethyl-1,4-oxathian S-oxides
✍ Scribed by J.C. Carretero; J.L. García Ruano; J.H. Rodríguez
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 248 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The stereoespecific syntheses of cis-and trans-2,3-dimethyl-1,4-oxathian, their diastereomeric --. S-oxides and their S-dioxide derivatives are reported. The key step in the synthetic pathways is the cyclization ofa 2-hydroxyalkyl vinylsulphoxide, by intramolecular conjugated addition with retention of configuration in the C and S chiral centers.
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in 80-95% yreld. Selective derivadzadon at rhe 5-andlor 7-positrons of 6-alkyl-1 ,I-dbnerhyl-I ,2,3.4-lerrahydronlenes was aclueved by As part of a systematic search for herbicidal compounds, a series of substituted 6-alkyl-l,l-dimethyl-1,2,3,4-tetrahydronaphthalenes were prepared. This project star