Abstract
AbstractWe describe the Sumitomo Chemical Company computer program, which designs synthetic routes for organic molecules, without consulting a user. There are only approximately 2500 reactions stored in the program. Significant advances in the automation of reaction input are presented. We also give some examples of synthetic routes proposed by the program, one being an enantiospecific and stereospecific route for the synthesis of the antibiotic chloramphenicol.
References
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Dates
Type | When |
---|---|
Created | 14 years, 11 months ago (Sept. 13, 2010, 9:02 p.m.) |
Deposited | 1 year, 10 months ago (Oct. 23, 2023, 1:57 p.m.) |
Indexed | 1 year, 10 months ago (Oct. 24, 2023, 7:28 p.m.) |
Issued | 33 years, 7 months ago (Jan. 1, 1992) |
Published | 33 years, 7 months ago (Jan. 1, 1992) |
Published Online | 14 years, 11 months ago (Sept. 2, 2010) |
Published Print | 33 years, 7 months ago (Jan. 1, 1992) |
@article{Dogane_1992, title={Computer‐executed synthesis planning, a progress report}, volume={111}, ISSN={0165-0513}, url={http://dx.doi.org/10.1002/recl.19921110606}, DOI={10.1002/recl.19921110606}, number={6}, journal={Recueil des Travaux Chimiques des Pays-Bas}, publisher={Wiley}, author={Dogane, I. and Takabatake, T. and Bersohn, M.}, year={1992}, month=jan, pages={291–296} }