Rearrangements Concerted with Fragmentation of Cyclopropylmethoxychlorocarbene and Cyclobutoxychlorocarbene in Hydrocarbon Solvents and Ar Matrices
Author:
Affiliation:
1. Contribution from the Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, New Brunswick, New Jersey 08903, and Department of Chemistry, University of Fribourg, Pérolles, CH-1700 Fribourg, Switzerland
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja049421x
Reference49 articles.
1. Small-ring Compounds. XXIII. The Nature of the Intermediates in Carbonium Ion-type Interconversion Reactions of Cyclopropylcarbinyl, Cyclobutyl and Allylcarbinyl Derivatives1a
2. Small-Ring Compounds. XXXII. The Reaction of Allylcarbinylamine-α-14C (3-Butenyl-1-14C-amine) with Nitrous Acid1,2
3. Lowry, T. H.; Richardson, K. S.Mechanism and Theory in Organic Chemistry, 3rd ed.; Harper and Row: New York, 1987; pp 454−463.
4. The preparation and some reactions of cyclopropyldiazomethane and cyclopropylmethyldiazotate
5. The Synthesis and Some Reactions of Diazocyclobutane1
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