Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
July 1, 1993Angewandte Chemie International Edition in English

Structural Evidence of the Aromaticity of Borepins: A Comparison of 1‐Chloroborepin and Tricarbonyl(1‐chloroborepin)molybdenum

View Full Paper
Ask AI
Bookmark
Share

Authors

AAArthur J. AsheUniversity of MichiganJKJeff W. KampfUniversity of MichiganWKWolfram KleinUniversity of Michigan

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Ashe et al. (1993) studied this question.

synapsesocial.com/papers/6a72a80bfebe604dd70ab58chttps://doi.org/10.1002/anie.199310651
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Aromatic Boron Heterocycles: The Generation of 1 H‐Borepin and the Structure of Tricarbonyl(1‐phenylborepin)molybdenum1992 · 58 citations
  2. 2Microwave Spectrum of 1,3,5-Cycloheptatriene1965 · 57 citations
  3. 3The First Synthesis of a Benzoborole1987 · 24 citations
  4. 4Conformational preferences and rotational barriers in polyene-ML3 transition metal complexes1977 · 282 citations
  5. 5Rearrangements of organometallic compounds. XIII. Boraaromatic systems. IV. Synthesis of heptaphenylborepin via the thermal rearrangement of heptaphenyl-7-borabicyclo[2.2.1]heptadiene1975 · 147 citations