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- W2950658889 abstract "Abstract Diazomethane adds in two directions to R 2 C=S, R = ethyl, propyl, isopropyl, tert -butyl; the dependence of the regioisomer ratio on R and on solvent polarity discloses the nature of the orienting forces. The thione- S -methylides generated by N 2 extrusion from 1,3,4-thiadiazolines undergo 1,4-H shift or electrocyclization." @default.
- W2950658889 created "2019-06-27" @default.
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- W2950658889 date "1990-07-24" @default.
- W2950658889 modified "2023-09-27" @default.
- W2950658889 title "ChemInform Abstract: Open-Chain Aliphatic Thiones and Diazomethane. Reactions of 1,3,4-Thiadiazolines and Thiocarbonyl Ylides." @default.
- W2950658889 cites W2024469640 @default.
- W2950658889 doi "https://doi.org/10.1002/chin.199030170" @default.
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