ChemInform Abstract: S‐[3‐Cyano‐2‐oxo‐3‐ (triphenyl‐λ<sup>5</sup>‐phosphanylidene)propyl] O‐Ethyl Carbonodithioate: A Novel Xanthate Reagent for the Synthesis of α‐Keto (Cyanomethylene)triphenylphosphorane Ylides from Olefins.

Lee, Kieseung

doi:10.1002/chin.201418198

ChemInform

2014

DOI: 10.1002/chin.201418198

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ChemInform Abstract: S‐[3‐Cyano‐2‐oxo‐3‐ (triphenyl‐λ⁵‐phosphanylidene)propyl] O‐Ethyl Carbonodithioate: A Novel Xanthate Reagent for the Synthesis of α‐Keto (Cyanomethylene)triphenylphosphorane Ylides from Olefins.

Kieseung Lee

Abstract: The novel xanthate reagent (I) can undergo group transfer addition to olefins (II) under radical conditions furnishing a concise access to α‐Keto ylides (IV).

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ChemInform Abstract: S‐[3‐Cyano‐2‐oxo‐3‐ (triphenyl‐λ⁵‐phosphanylidene)propyl] O‐Ethyl Carbonodithioate: A Novel Xanthate Reagent for the Synthesis of α‐Keto (Cyanomethylene)triphenylphosphorane Ylides from Olefins.

Abstract: The novel xanthate reagent (I) can undergo group transfer addition to olefins (II) under radical conditions furnishing a concise access to α‐Keto ylides (IV).

Cited by 0 publications

References 1 publication

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ChemInform Abstract: S‐[3‐Cyano‐2‐oxo‐3‐ (triphenyl‐λ5‐phosphanylidene)propyl] O‐Ethyl Carbonodithioate: A Novel Xanthate Reagent for the Synthesis of α‐Keto (Cyanomethylene)triphenylphosphorane Ylides from Olefins.

Abstract: The novel xanthate reagent (I) can undergo group transfer addition to olefins (II) under radical conditions furnishing a concise access to α‐Keto ylides (IV).

Cited by 0 publications

References 1 publication

No citations

Contact Info

Product

Resources

About

ChemInform Abstract: S‐[3‐Cyano‐2‐oxo‐3‐ (triphenyl‐λ⁵‐phosphanylidene)propyl] O‐Ethyl Carbonodithioate: A Novel Xanthate Reagent for the Synthesis of α‐Keto (Cyanomethylene)triphenylphosphorane Ylides from Olefins.