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1983, Francis A. Carey, Richard J. Sundberg, Advanced Organic Chemistry: Reactions and synthesis, Plenum Press, page 578,
The retrosyntheses shown in Scheme 11.11 correspond to the syntheses in Schemes 11.12 and 11.13.
1991, Australian Journal of Chemistry, Volume 44, CSIRO, page 1294:
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).
2007, Helmut Cölfen, “Bio-inspired Mineralization Using Hydrophilic Polymers”, in Kensuke Naka, editor, Biomineralization II: Mineralization Using Synthetic Polymers and Templates, Springer, page 25:
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.
Retrosynthetic analysis on Wikipedia.Wikipedia 