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020 |a9783034857888|9978-3-0348-5788-8
024 7 |a10.1007/978-3-0348-5788-8|2doi
041 |aeng
049 |aTürk Tarih Kurumu Kütüphanesi
050 4|aH1-99
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090 |aDK/8685
100 1 |aDAVIS.|eauthor.|4aut|4http://id.loc.gov/vocabulary/relators/aut
245 10|aComputer Representation of the Stereochemistry of Organic Molecules|h[electronic resource] :|bWith application to the problem of discovery of organic synthesis by computer /|cby DAVIS.
250 |a1st ed. 1976.
264 1|aBasel :|bBirkhäuser Basel :|bImprint: Birkhäuser,|c1976.
300 |aXII, 132 p.|bonline resource.
336 |atext|btxt|2rdacontent
337 |acomputer|bc|2rdamedia
338 |aonline resource|bcr|2rdacarrier
347 |atext file|bPDF|2rda
490 1 |aInterdisciplinary Systems Research
505 0 |aConstitutional Equivalence -- Identifying and Numbering the CE Classes: Algorithm 1 -- The Canonical TSD: Algorithm 2 -- Stereochemical Equivalence and the Canonical Parity Vector -- Identifying and Numbering the SE Classes.
520 |aThe role of the computer in the practice of organic chemistry has been firmly established over the past decade. Its uses as a large scale information storage and retrieval device in chemistry have been too numerous to mention. More recently, the applicability of computers to the problem of discovering valid and reasonable synthesis routes for organic molecules has been demonstrated. This has been both as an adjunct to the 1 chemist in the on-line interactive mode ,2,3 and also as a wholly computer-directed system seeking to simulate the intelligent prob- 4 lem-solving activity of the human organic synthetic chemist. ,5 In all of these computer applications to organic chemistry, it has been necessary to devise some computer-compatible repres- tation of an organic molecule that is both canonical and c- venient for table look-ups. This is in order that entities that have been constructed at different times under different circumstances can be identified and classified, with identical molecules being recognized as such even if their connection matrices list the elements of the molecule in different orders. E. J. Corey and W. T. Wipke, Science, 166, 178 (1969). 2 E. J. Corey, W. T. Wipke, R. D. Cramer III and W. J. Howe, J. Americ. Chern. Soc. , 94, 421 (1972) and 431 (1972). 3 E. J. Corey, R. D. Cramer III and W. J. Howe, ~. Americ. Chern. Soc. , 94, 440 (1972). 4 H. L. Gelernter, N. S. Sridharan and A. J.
532 8 |aAccessibility summary: This PDF is not accessible. It is based on scanned pages and does not support features such as screen reader compatibility or described non-text content (images, graphs etc). However, it likely supports searchable and selectable text based on OCR (Optical Character Recognition). Users with accessibility needs may not be able to use this content effectively. Please contact us at accessibilitysupport@springernature.com if you require assistance or an alternative format.
532 8 |aInaccessible, or known limited accessibility
532 8 |aNo reading system accessibility options actively disabled
532 8 |aPublisher contact for further accessibility information: accessibilitysupport@springernature.com
650 0|aSocial sciences.
650 0|aHumanities.
650 14|aHumanities and Social Sciences.
710 2 |aSpringerLink (Online service)
773 0 |tSpringer Nature eBook
776 08|iPrinted edition:|z9783764308476
776 08|iPrinted edition:|z9783034857895
830 0|aInterdisciplinary Systems Research
856 40|uhttps://doi.org/10.1007/978-3-0348-5788-8
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912 |aZDB-2-SXH
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950 |aHumanities, Social Sciences and Law (SpringerNature-11648)
950 |aHistory (R0) (SpringerNature-43722)