ChemInform Abstract: Selective Formation of Five‐Membered Heterocyclic Products by Anodic Oxidation of Alkyl Isothiocyanates (RNCS) in Dichloromethane and Their Thermal Isomerization and Decomposition.

Becker, James Y.; Yatziv, Shimon

doi:10.1002/chin.198840173

ChemInform

1988

DOI: 10.1002/chin.198840173

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ChemInform Abstract: Selective Formation of Five‐Membered Heterocyclic Products by Anodic Oxidation of Alkyl Isothiocyanates (RNCS) in Dichloromethane and Their Thermal Isomerization and Decomposition.

James Y. Becker

Shimon Yatziv

Abstract: Anodic oxidation of the alkyl isothiocyanates (I) in dichloromethane yields the dithiazolidine‐3‐ones (II) and the thiadiazolidine‐3‐thiones (IIIa) and (IIIb).

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ChemInform Abstract: Selective Formation of Five‐Membered Heterocyclic Products by Anodic Oxidation of Alkyl Isothiocyanates (RNCS) in Dichloromethane and Their Thermal Isomerization and Decomposition.

Abstract: Anodic oxidation of the alkyl isothiocyanates (I) in dichloromethane yields the dithiazolidine‐3‐ones (II) and the thiadiazolidine‐3‐thiones (IIIa) and (IIIb).

Cited by 0 publications

References 1 publication

No citations

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