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    <responseDate>2026-10-11T06:10:57Z</responseDate>
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    <identifier>10.57760/sciencedb.20895</identifier>
    <datestamp>2025-02-14T15:00:36Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2025-02-14</dc:date>
  <dc:title>FID - Dual Methylene Group Transfer</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.20895</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>NMR spectra were acquired on Bruker Avance 400 and Bruker Avance 600 spectrometers at room temperature; the chemical shifts d were measured in ppm with respect to solvent (1Н:&amp;nbsp;CDCl3, &amp;delta; = 7.26 ppm; DMSO-d6: &amp;delta; = 2.50 ppm; 13C: CDCl3, &amp;delta; = 77.2 ppm; DMSO-d6: &amp;delta; = 39.5 ppm). Splitting patterns are designated as s, singlet; d, doublet; t, triplet; m, multiplet; dd, double doublet; ddd, double double doublet; dddd, double double double doublet. Coupling constants (J) are given in Hertz.</dc:description>
  <dc:subject>NMR spectra ; benzylcyclopropane ; Cyclopropanation and Epoxidation</dc:subject>
  <dc:creator>Vitaly V. Shorokhov</dc:creator>
  <dc:creator>Beauty K. Chabuka</dc:creator>
  <dc:creator>Albina A. Nikolaeva</dc:creator>
  <dc:creator>Sergey S. Zhokhov</dc:creator>
  <dc:creator>Ivan A. Andreev</dc:creator>
  <dc:creator>Nina K. Ratmanova</dc:creator>
  <dc:creator>Igor V. Trushkov</dc:creator>
  <dc:creator>Olga A. Ivanova</dc:creator>
  <dc:creator>Igor V. Alabugin</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/publicdomain/zero/1.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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