See retrosynthesis in All languages combined, or Wiktionary
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"text": "1983, Francis A. Carey, Richard J. Sundberg, Advanced Organic Chemistry: Reactions and synthesis, Plenum Press, page 578,\nThe retrosyntheses shown in Scheme 11.11 correspond to the syntheses in Schemes 11.12 and 11.13."
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"ref": "1991, Australian Journal of Chemistry, Volume 44, CSIRO, page 1294:",
"text": "The retrosyntheses shown in Scheme 2 lead directly to acetylene-type retrons (14)-(16) (path a) or implicate the use of Dewar o-xylylene (17) (path b) and the smaller retrons (18)-(20); the latter path was the route we elected to pursue (Scheme 3).",
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"ref": "2007, Helmut Cölfen, “Bio-inspired Mineralization Using Hydrophilic Polymers”, in Kensuke Naka, editor, Biomineralization II: Mineralization Using Synthetic Polymers and Templates, Springer, page 25:",
"text": "For example, the above mentioned retrosynthesis of nacre [132] is as much bio-inspired as is the crystallization in presence of hydrophilic polymers [44], although in the first case, the original biomineral structure is reproduced, whereas in the latter case, no biomineral is reproduced but complex crystal morphologies are obtained.",
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This page is a part of the kaikki.org machine-readable English dictionary. This dictionary is based on structured data extracted on 2024-11-06 from the enwiktionary dump dated 2024-10-02 using wiktextract (fbeafe8 and 7f03c9b). 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.
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