{"doi":"10.1246/bcsj.49.2522","title":"A New Type of Induced Decomposition. III Induced Decomposition of Cinnamoyl Peroxide, <i>t</i>-Butyl Peroxycinnamate and <i>t</i>-Butyl 2,3-Diphenylperoxypropionate in Solution","abstract":"<jats:title>Abstract</jats:title>\n               <jats:p>Phenyl and benzyl radicals were found to induce decomposition of cinnamoyl peroxide or t-butylperoxycinnamate to give stilbene and 1,3-diphenylpropene, respectively. Similarly, t-butoxyl radicals caused t-butyl 2,3-diphenylperoxypropionate to decompose affording stilbene. A mechanism is proposed which involves a radical atttack on a substrate peroxide producing a radical carrying an odd electron on the carbon atom β to the carboxyl group and its subsequent collapse to final products by way of β-scission.</jats:p>","journal":"Bulletin of the Chemical Society of Japan","year":1976,"id":30036,"datarank":0.2627748522228322,"base_score":1.6094379124341003,"endowment":1.6094379124341003,"self_citation_contribution":0.24141568686511508,"citation_network_contribution":0.021359165357717112,"self_endowment_contribution":0.24141568686511508,"citer_contribution":0.021359165357717112,"corpus_percentile":null,"corpus_rank":null,"citation_count":4,"citer_count":1,"citers_with_citation_signal":1,"citers_with_endowment":1,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":164162,"name":"Yoshitsugu Usuda","orcid":null,"position":1,"is_corresponding":false},{"id":164163,"name":"Masayuki Yoshida","orcid":null,"position":2,"is_corresponding":false},{"id":164164,"name":"Osamu Simamura","orcid":null,"position":3,"is_corresponding":false},{"id":164160,"name":"Tameichi Ochiai","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"base_score":1.6094379124341003,"endowment":1.6094379124341003,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"18998881","pmcid":null,"openalex_id":"https://openalex.org/W1972003847","authors":[],"funders":[],"total_grants":0,"fwci":1.8124,"citation_percentile":0.78764185,"influential_citations":0,"citation_trend":[],"oa_status":"closed","license":"https://academic.oup.com/pages/standard-publication-reuse-rights","oa_locations":[{"url":"https://doi.org/10.1246/bcsj.49.2522","host_type":"CLOSED"},{"url":"https://academic.oup.com/bcsj/article-pdf/49/9/2522/56094369/bcsj.49.2522.pdf","host_type":"publisher"}],"fields_of_study":["Free Radicals and Antioxidants","Radical Photochemical Reactions","Photochemistry and Electron Transfer Studies","Chemistry"],"mesh_terms":[],"keywords":["Chemistry","Radical","Decomposition","Peroxide","Carbon atom","Substrate (aquarium)","Medicinal chemistry","Photochemistry","Organic peroxide","Chemical decomposition","Hydrogen peroxide","Polymer chemistry","Organic chemistry","Ring (chemistry)"],"sdg_mappings":[],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-06-09T01:40:44.192877Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}