{"doi":"10.1002/crat.200410436","title":"Configuration, conformation and crystal structure of rabdosianin b","abstract":null,"journal":"Crystal Research and Technology","year":2005,"id":588247,"datarank":0.5871779580748375,"base_score":1.0986122886681096,"endowment":1.0986122886681096,"self_citation_contribution":0.16479184330021646,"citation_network_contribution":0.42238611477462107,"self_endowment_contribution":0.16479184330021646,"citer_contribution":0.42238611477462107,"corpus_percentile":null,"corpus_rank":null,"citation_count":2,"citer_count":2,"citers_with_citation_signal":2,"citers_with_endowment":2,"datacite_reuse_total":1,"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":1504876,"name":"Yuan Jiang Pan","orcid":null,"position":1,"is_corresponding":false},{"id":673866,"name":"Jin Li","orcid":"0000-0002-7957-1476","position":2,"is_corresponding":false},{"id":904789,"name":"Ling Tong","orcid":"0000-0001-5038-5197","position":3,"is_corresponding":false},{"id":1445834,"name":"Kai Bei Yu","orcid":null,"position":4,"is_corresponding":false},{"id":1504875,"name":"Bao Lin Li","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"resolved":true,"title":"Configuration, conformation and crystal structure of rabdosianin b","abstract":"Rabdosianin B, 7,20-epoxy-7β-hydroxy-1α,6β,11α,15β-tetraacetoxy-ent-kaur-16-ene, C28H38O10, was the first isolated from Isodon henryi. It consists of three six-membered rings A, B, C and one five-membered ring D. The fused-ring system A, B and C are in chair, boat and chair conformations, respectively, and ring D is in an envelope conformation, on the basis of NMR and X-ray diffraction analysis. The crystal of rabdosianin B is in orthorhombic crystal system with space group P212121, lattice constants: a = 9.969(1) Å, b = 15.400(3) Å, and c = 17.624(3) Å, Z = 4. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)","is_dataset_classified":null,"base_score":1.0986122886681096,"endowment":1.0986122886681096,"datacite_reuse_total":1,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"20725694","pmcid":null,"openalex_id":"https://openalex.org/W2074647356","authors":[],"funders":[],"total_grants":0,"fwci":0.1256,"citation_percentile":0.50401414,"influential_citations":0,"citation_trend":[{"year":2023,"count":1}],"oa_status":"closed","license":"http://doi.wiley.com/10.1002/tdm_license_1.1","oa_locations":[{"url":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fcrat.200410436","host_type":"publisher"},{"url":"https://onlinelibrary.wiley.com/doi/full/10.1002/crat.200410436","host_type":"publisher"},{"url":"https://doi.org/10.1002/crat.200410436","host_type":"journal"}],"fields_of_study":["Bioactive Natural Diterpenoids Research","Plant-based Medicinal Research","Advanced Synthetic Organic Chemistry"],"mesh_terms":[],"keywords":["Orthorhombic crystal system","Ring (chemistry)","Crystal structure","Crystallography","Cyclohexane conformation","Chemistry","Stereochemistry","Lattice constant","Envelope (radar)","Diffraction","Molecule","Physics","Hydrogen bond","Optics","Organic chemistry"],"sdg_mappings":[{"sdg_number":0,"sdg_label":"Life below water"}],"linked_datasets":[{"doi":"10.5517/cc76xv5","title":"CCDC 215197: Experimental Crystal Structure Determination","publisher":"Cambridge Crystallographic Data Centre","resource_type":"Dataset"}],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-07-19T22:15:54.721295Z","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":[]}