000 02984nam a2200385 i 4500
008 950327s2007 enka b 001 0 eng
020 _a0198557914
_q(pbk.)
020 _a9780198557913
_q(pbk.)
035 _a(OCoLC)32347523
_z(OCoLC)33042285
_z(OCoLC)877339400
040 _aDLC
_beng
_cDLC
_dC#P
_dUKM
_dNLGGC
_dBAKER
_dBTCTA
_dYDXCP
_dBMU
_dUBC
_dZWZ
_dBDX
_dOCLCO
_dOCLCF
_dNLE
_dOCLCQ
_dUtOrBLW
_dBAUN
049 _aBAUN_MERKEZ
050 0 4 _aQD262
_b.W53 2007
082 0 0 _220
100 1 _aWillis, Christine L
245 1 0 _aOrganic synthesis /
_cChristine L. Willis, Martin Wills
264 1 _aOxford ;
_aNew York :
_bOxford University Press,
_c2007
300 _a91 pages :
_billustrations ;
_c25 cm
336 _atext
_btxt
_2rdacontent
337 _aunmediated
_bn
_2rdamedia
338 _avolume
_bnc
_2rdacarrier
490 1 _aOxford chemistry primers ;
_v31
490 1 _aOxford science publications
504 _aIncludes bibliographical references and index
505 0 0 _tIntroduction to synthesis
_t-- Retrosynthetic analysis: I, the basic concepts; II, latent polarity and FGIs; III, strategy and planning Selectivity: I, chemoselectivity and protecting groups; II, regioselectivity; III, stereoselectivity
_t-- Selected organic syntheses
520 _aThis series of short texts provides accessible accounts of a range of essential topics in chemistry. Written with the needs of the student in mind, the Oxford Chemistry Primers offer just the right level of detail for undergraduate study, and will be invaluable as a source of material commonly presented in lecture courses yet not adequately covered in existing texts. All the basic principles and facts in a particular area are presented in a clear and straightforward style, to produce concise yet comprehensive accounts of topics covered in both core and specialist courses. This book introduces a logical approach for the design of synthetic routes to reasonably complex organic molecules from simple starting materials. It describes the concept of 'retrosynthesis', which allows suitable simple starting materials to be identified; the importance of bond polarity and functional group interconversions; how to find an effective route to a target molecule containing more than one functional group; and valuable strategies to adopt when designing syntheses. The text also includes a review of methods for the control of chemo-, regio-, and stereoselectivity, and a discussion of protecting groups. Finally four syntheses of the pyrrolidine alkaloids are compared and contrasted using the principles described in the book. Practice examples are provided throughout the book
650 0 _aOrganic compounds
_xSynthesis
653 0 _aOrganic compounds
_aSynthesis
700 1 _aWills, Martin
710 2 _9111967
_aOxford University Press.
830 0 _9108617
_aOxford chemistry primers ;
_v31
830 0 _969018
_aOxford science publications.
900 _a23642
900 _bsatın
942 _2lcc
_cKT
999 _c19243
_d19243