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Access to Complex Scaffolds Through [2 + 2] Cycloadditions of Strained Cyclic Allenes.
McVeigh, Matthew S; Sorrentino, Jacob P; Hands, Allison T; Garg, Neil K.
Affiliation
  • McVeigh MS; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States.
  • Sorrentino JP; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States.
  • Hands AT; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States.
  • Garg NK; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States.
J Am Chem Soc ; 146(22): 15420-15427, 2024 Jun 05.
Article in En | MEDLINE | ID: mdl-38768558
ABSTRACT
We report the strain-induced [2 + 2] cycloadditions of cyclic allenes for the assembly of highly substituted cyclobutanes. By judicious choice of trapping agent, complex scaffolds bearing heteroatoms, fused rings, contiguous stereocenters, spirocycles, and quaternary centers are ultimately accessible. Moreover, we show that the resulting cycloadducts can undergo thermal isomerization. This study provides an alternative strategy to photochemical [2 + 2] cycloadditions for accessing highly functionalized cyclobutanes, while validating the use of underexplored strained intermediates for the assembly of complex architectures.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Chem Soc Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Chem Soc Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States