"tosylacetylene" meaning in All languages combined

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "tosyl",
        "3": "acetylene"
      },
      "expansion": "tosyl + acetylene",
      "name": "com"
    }
  ],
  "etymology_text": "tosyl + acetylene",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "tosylacetylene (uncountable)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        {
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
            "Entries with incorrect language header",
            "Entry maintenance"
          ],
          "source": "w"
        },
        {
          "kind": "topical",
          "langcode": "en",
          "name": "Organic chemistry",
          "orig": "en:Organic chemistry",
          "parents": [
            "Chemistry",
            "Sciences",
            "All topics",
            "Fundamental"
          ],
          "source": "w"
        }
      ],
      "examples": [
        {
          "ref": "2007, M. Green, Organometallic Chemistry, volume 31, page 222",
          "text": "This is regioselectively trapped in situ by the tosylacetylene 87 via one of two mechanisms to generate 88 or 89.",
          "type": "quotation"
        },
        {
          "ref": "2012, V. Nenajdenko, Isocyanide Chemistry: Applications in Synthesis and Material Science",
          "text": "[…] accomplished via the Diels–Alder reaction of tosylacetylene with butadiene […]",
          "type": "quotation"
        },
        {
          "ref": "2014, Johann Mulzer, Science of Synthesis, page 370",
          "text": "The addition of a thiol to tosylacetylene affords the corresponding tosylvinyl sulfide as a mixture of Z-and E-isomers (4:1) in excellent yields.",
          "type": "quotation"
        }
      ],
      "glosses": [
        "Ethynyl p-tolyl sulfone, C₉H₈O₂S, used as a reagent in a wide variety of applications."
      ],
      "id": "en-tosylacetylene-en-noun-mIC3kjRR",
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "Ethynyl",
          "ethynyl"
        ],
        [
          "p-",
          "p-"
        ],
        [
          "tolyl",
          "tolyl"
        ],
        [
          "sulfone",
          "sulfone"
        ],
        [
          "reagent",
          "reagent"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) Ethynyl p-tolyl sulfone, C₉H₈O₂S, used as a reagent in a wide variety of applications."
      ],
      "tags": [
        "uncountable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ]
    }
  ],
  "word": "tosylacetylene"
}

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "tosyl",
        "3": "acetylene"
      },
      "expansion": "tosyl + acetylene",
      "name": "com"
    }
  ],
  "etymology_text": "tosyl + acetylene",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "tosylacetylene (uncountable)",
      "name": "en-noun"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "noun",
  "senses": [
    {
      "categories": [
        "English compound terms",
        "English entries with incorrect language header",
        "English lemmas",
        "English nouns",
        "English terms with quotations",
        "English uncountable nouns",
        "Quotation templates to be cleaned",
        "en:Organic chemistry"
      ],
      "examples": [
        {
          "ref": "2007, M. Green, Organometallic Chemistry, volume 31, page 222",
          "text": "This is regioselectively trapped in situ by the tosylacetylene 87 via one of two mechanisms to generate 88 or 89.",
          "type": "quotation"
        },
        {
          "ref": "2012, V. Nenajdenko, Isocyanide Chemistry: Applications in Synthesis and Material Science",
          "text": "[…] accomplished via the Diels–Alder reaction of tosylacetylene with butadiene […]",
          "type": "quotation"
        },
        {
          "ref": "2014, Johann Mulzer, Science of Synthesis, page 370",
          "text": "The addition of a thiol to tosylacetylene affords the corresponding tosylvinyl sulfide as a mixture of Z-and E-isomers (4:1) in excellent yields.",
          "type": "quotation"
        }
      ],
      "glosses": [
        "Ethynyl p-tolyl sulfone, C₉H₈O₂S, used as a reagent in a wide variety of applications."
      ],
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "Ethynyl",
          "ethynyl"
        ],
        [
          "p-",
          "p-"
        ],
        [
          "tolyl",
          "tolyl"
        ],
        [
          "sulfone",
          "sulfone"
        ],
        [
          "reagent",
          "reagent"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) Ethynyl p-tolyl sulfone, C₉H₈O₂S, used as a reagent in a wide variety of applications."
      ],
      "tags": [
        "uncountable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ]
    }
  ],
  "word": "tosylacetylene"
}