ChemInform Abstract: Highly Stereoselective Radical Cyclization: Copper‐ or Ruthenium‐Catalyzed Preparation of cis‐ and trans‐β,γ‐Dialkyl γ‐Lactams from Acyclic N‐Allyltrichloroacetamide Derivatives.

H Nagashima,K Seki,K Itoh,M Ishii,N Ozaki

doi:10.1002/chin.199008136

ChemInform Abstract: Highly Stereoselective Radical Cyclization: Copper‐ or Ruthenium‐Catalyzed Preparation of cis‐ and trans‐β,γ‐Dialkyl γ‐Lactams from Acyclic N‐Allyltrichloroacetamide Derivatives.

H Nagashima, K Seki + Show 3 more

https://doi.org/10.1002/chin.199008136

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Journal: ChemInform

Publication Date: Feb 20, 1990

Affiliation: Toyohashi University of Technology

#Acyclic Derivatives #Stereoselective Radical Cyclization #Preparation Of Cis #Stereoselective Radical #Radical Cyclization

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AbstractCopper(I)‐catalyzed cyclization of the acetamides (I) yields the lactams (II) or (III) via 1,2‐asymmetric induction.

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ChemInform Abstract: Highly Stereoselective Radical Cyclization: Copper‐ or Ruthenium‐Catalyzed Preparation of cis‐ and trans‐β,γ‐Dialkyl γ‐Lactams from Acyclic N‐Allyltrichloroacetamide Derivatives.