Kinetic and Mechanistic Studies of the Formal (1+2)- and (1+4)-Cycloadditions of Germylenes to Conjugated Dienes
Author:
Affiliation:
1. Department of Chemistry and Chemical Biology, McMaster University, Hamilton ON L8S 4M1, Canada
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om900791e
Reference48 articles.
1. Germylenes and stannylenes
2. Tokitoh, N.; Ando, W.; Moss, R. A.; Platz, M. S.; Jones, M., Jr.InReactive Intermediate Chemistry;John Wiley & Sons:New York, 2004; pp651−715.
3. Carbene-Analogous Germylenes(Germandiyls): Singlets or Triplets?–The First Stereospecific Cycloadditions of R2Ge to Conjugated Dienes
4. Stereochemistry of dimetrylgermylene addition to E,E-and E,Z-2,4-hexadienes in the gas phase
5. Chemistry of heavy carbene analogs R2M (M = Si, Ge, Sn). 8. Germylenes: singlets or triplets? [2 + 4]Cheletropic cycloadditions of dimethylgermylene and diiodogermylene to conjugated dienes
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