000			02091nam a2200301Ia 4500
003			OSt
005			20250807105302.0
008			220909b |||||||| |||| 00| 0 eng d
020			_a9780470712368
037			_cTextbook
040			_aCSL _beng _cCSL
041			_aeng
084			_aE5:4 M2;P8;12 TE _qCSL
100			_aWarren Stuart _eauthor
245		0	_aOrganic synthesis _b: the disconnection approach.
250			_a2nd ed.
260			_aWest Sussex : _bWiley, _c2008.
300			_aviii, 329p. _b: ill.
500			_aIndex 325-329p.; Reprint 2014.
520			_aOne approach to organic synthesis is retrosynthetic analysis. With this approach a chemist will start with the structure of their target molecule and progressively cut bonds to create simpler molecules. Reversing this process gives a synthetic route to the target molecule from simpler starting materials. This “disconnection” approach to synthesis is now a fundamental part of every organic synthesis course. Organic Synthesis: The Disconnection Approach, 2nd Edition introduces this important technique, to help students to design their own organic syntheses. There are forty chapters: those on the synthesis of given types of molecules alternate with strategy chapters in which the methods just learnt are placed in a wider context. The synthesis chapters cover many ways of making each type of molecule starting with simple aromatic and aliphatic compounds with one functional group and progressing to molecules with many functional groups. The strategy chapters cover questions of selectivity, protection, stereochemistry, and develop more advanced thinking via reagents specifically designed for difficult problems.
650			_a Chemoselectivity _9817391
650			_a Difunctionalised compounds _9817392
650			_a Stereoselectivity _9817393
650			_aTwo-group _9817388
700			_aWyatt, Paul _eco-author
942			_hE5:4 M2;P8;12 TE _cTB _2CC _n0
999			_c16936 _d16936