"stereodivergent" meaning in English

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "stereo",
        "3": "divergent"
      },
      "expansion": "stereo- + divergent",
      "name": "prefix"
    }
  ],
  "etymology_text": "stereo- + divergent",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "stereodivergent (not comparable)",
      "name": "en-adj"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "adj",
  "senses": [
    {
      "categories": [
        {
          "kind": "other",
          "name": "English entries with incorrect language header",
          "parents": [
            "Entries with incorrect language header",
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          "source": "w"
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        {
          "kind": "other",
          "name": "English terms prefixed with stereo-",
          "parents": [],
          "source": "w"
        },
        {
          "kind": "topical",
          "langcode": "en",
          "name": "Organic chemistry",
          "orig": "en:Organic chemistry",
          "parents": [
            "Chemistry",
            "Sciences",
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            "Fundamental"
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          "source": "w"
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      ],
      "examples": [
        {
          "ref": "2015 June 10, Ruth Dorel, Antonio M. Echavarren, “Gold-Catalyzed Reactions via Cyclopropyl Gold Carbene-like Intermediates”, in The Journal of Organic Chemistry, volume 80, →DOI",
          "text": "This cascade cyclization process is ideally suited for the total syntheses of sesquiterpenes (−)-4α,7α-aromadendranediol ( 92 ), (−)-4β,7α-aromadendranediol ( 93 ), and (−)-epiglobulol ( 94 ) from a single dienyne 84b by using a stereodivergent gold(I)-catalyzed reaction as the key step (Scheme 24 ). 115 In the absence of any external nucleophile, cyclopropyl gold(I) carbene intermediate 89 undergoes a 1,5-OBn migration followed by intramolecular cyclopropanation to form tricyclic compound 88b, which is the precursor of 93 and 94 .",
          "type": "quotation"
        }
      ],
      "glosses": [
        "That produces different chiral forms of the same compound"
      ],
      "id": "en-stereodivergent-en-adj-I88WRmi8",
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "different",
          "different"
        ],
        [
          "chiral",
          "chiral"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) That produces different chiral forms of the same compound"
      ],
      "related": [
        {
          "word": "stereodivergence"
        }
      ],
      "tags": [
        "not-comparable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ]
    }
  ],
  "word": "stereodivergent"
}

{
  "etymology_templates": [
    {
      "args": {
        "1": "en",
        "2": "stereo",
        "3": "divergent"
      },
      "expansion": "stereo- + divergent",
      "name": "prefix"
    }
  ],
  "etymology_text": "stereo- + divergent",
  "head_templates": [
    {
      "args": {
        "1": "-"
      },
      "expansion": "stereodivergent (not comparable)",
      "name": "en-adj"
    }
  ],
  "lang": "English",
  "lang_code": "en",
  "pos": "adj",
  "related": [
    {
      "word": "stereodivergence"
    }
  ],
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        "en:Organic chemistry"
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      "examples": [
        {
          "ref": "2015 June 10, Ruth Dorel, Antonio M. Echavarren, “Gold-Catalyzed Reactions via Cyclopropyl Gold Carbene-like Intermediates”, in The Journal of Organic Chemistry, volume 80, →DOI",
          "text": "This cascade cyclization process is ideally suited for the total syntheses of sesquiterpenes (−)-4α,7α-aromadendranediol ( 92 ), (−)-4β,7α-aromadendranediol ( 93 ), and (−)-epiglobulol ( 94 ) from a single dienyne 84b by using a stereodivergent gold(I)-catalyzed reaction as the key step (Scheme 24 ). 115 In the absence of any external nucleophile, cyclopropyl gold(I) carbene intermediate 89 undergoes a 1,5-OBn migration followed by intramolecular cyclopropanation to form tricyclic compound 88b, which is the precursor of 93 and 94 .",
          "type": "quotation"
        }
      ],
      "glosses": [
        "That produces different chiral forms of the same compound"
      ],
      "links": [
        [
          "organic chemistry",
          "organic chemistry"
        ],
        [
          "different",
          "different"
        ],
        [
          "chiral",
          "chiral"
        ]
      ],
      "raw_glosses": [
        "(organic chemistry) That produces different chiral forms of the same compound"
      ],
      "tags": [
        "not-comparable"
      ],
      "topics": [
        "chemistry",
        "natural-sciences",
        "organic-chemistry",
        "physical-sciences"
      ]
    }
  ],
  "word": "stereodivergent"
}