See Weiss-Cook reaction on Wiktionary
{ "etymology_text": "Named after U. Weiss and his student J. M. Cook.", "forms": [ { "form": "the Weiss-Cook reaction", "tags": [ "canonical" ] } ], "head_templates": [ { "args": { "def": "1" }, "expansion": "the Weiss-Cook reaction", "name": "en-prop" } ], "lang": "English", "lang_code": "en", "pos": "name", "senses": [ { "categories": [ { "kind": "other", "name": "English entries with incorrect language header", "parents": [ "Entries with incorrect language header", "Entry maintenance" ], "source": "w" }, { "kind": "other", "name": "Pages with 1 entry", "parents": [], "source": "w" }, { "kind": "other", "name": "Pages with entries", "parents": [], "source": "w" }, { "kind": "topical", "langcode": "en", "name": "Chemical processes", "orig": "en:Chemical processes", "parents": [ "Nature", "All topics", "Fundamental" ], "source": "w" }, { "kind": "topical", "langcode": "en", "name": "Chemical reactions", "orig": "en:Chemical reactions", "parents": [ "Chemistry", "Sciences", "All topics", "Fundamental" ], "source": "w" }, { "kind": "topical", "langcode": "en", "name": "Organic chemistry", "orig": "en:Organic chemistry", "parents": [ "Chemistry", "Sciences", "All topics", "Fundamental" ], "source": "w" } ], "glosses": [ "The synthesis of cis-bicyclo[3.3.0]octane-3,7-dione employing an acetonedicarboxylic acid ester and a diacyl (1,2 ketone); it operates in the same way as the Knoevenagel condensation." ], "id": "en-Weiss-Cook_reaction-en-name-KGPOL2GH", "links": [ [ "organic chemistry", "organic chemistry" ], [ "synthesis", "synthesis" ], [ "acetonedicarboxylic acid", "acetonedicarboxylic acid" ], [ "ester", "ester" ], [ "diacyl", "diacyl" ], [ "ketone", "ketone" ], [ "Knoevenagel condensation", "Knoevenagel condensation" ] ], "raw_glosses": [ "(organic chemistry) The synthesis of cis-bicyclo[3.3.0]octane-3,7-dione employing an acetonedicarboxylic acid ester and a diacyl (1,2 ketone); it operates in the same way as the Knoevenagel condensation." ], "topics": [ "chemistry", "natural-sciences", "organic-chemistry", "physical-sciences" ] } ], "word": "Weiss-Cook reaction" }
{ "etymology_text": "Named after U. Weiss and his student J. M. Cook.", "forms": [ { "form": "the Weiss-Cook reaction", "tags": [ "canonical" ] } ], "head_templates": [ { "args": { "def": "1" }, "expansion": "the Weiss-Cook reaction", "name": "en-prop" } ], "lang": "English", "lang_code": "en", "pos": "name", "senses": [ { "categories": [ "English entries with incorrect language header", "English eponyms", "English lemmas", "English multiword terms", "English proper nouns", "English uncountable nouns", "Pages with 1 entry", "Pages with entries", "en:Chemical processes", "en:Chemical reactions", "en:Organic chemistry" ], "glosses": [ "The synthesis of cis-bicyclo[3.3.0]octane-3,7-dione employing an acetonedicarboxylic acid ester and a diacyl (1,2 ketone); it operates in the same way as the Knoevenagel condensation." ], "links": [ [ "organic chemistry", "organic chemistry" ], [ "synthesis", "synthesis" ], [ "acetonedicarboxylic acid", "acetonedicarboxylic acid" ], [ "ester", "ester" ], [ "diacyl", "diacyl" ], [ "ketone", "ketone" ], [ "Knoevenagel condensation", "Knoevenagel condensation" ] ], "raw_glosses": [ "(organic chemistry) The synthesis of cis-bicyclo[3.3.0]octane-3,7-dione employing an acetonedicarboxylic acid ester and a diacyl (1,2 ketone); it operates in the same way as the Knoevenagel condensation." ], "topics": [ "chemistry", "natural-sciences", "organic-chemistry", "physical-sciences" ] } ], "word": "Weiss-Cook reaction" }
Download raw JSONL data for Weiss-Cook reaction meaning in All languages combined (1.4kB)
This page is a part of the kaikki.org machine-readable All languages combined dictionary. This dictionary is based on structured data extracted on 2024-12-21 from the enwiktionary dump dated 2024-12-04 using wiktextract (d8cb2f3 and 4e554ae). The data shown on this site has been post-processed and various details (e.g., extra categories) removed, some information disambiguated, and additional data merged from other sources. See the raw data download page for the unprocessed wiktextract data.
If you use this data in academic research, please cite Tatu Ylonen: Wiktextract: Wiktionary as Machine-Readable Structured Data, Proceedings of the 13th Conference on Language Resources and Evaluation (LREC), pp. 1317-1325, Marseille, 20-25 June 2022. Linking to the relevant page(s) under https://kaikki.org would also be greatly appreciated.