000			02104nam a2200181Ia 4500
008			140223b2008 xxu||||| |||| 00| 0 eng d
020			_a9783527306848 _c0.00
082			_a541.39 _bNIC
100			_aNicolaou, K. C.
245			_aClassic in Total Synthesis II: MoreTargets, Strategies and Methods
260			_aNew York _bVCH: A Wiley Company _c2008
300			_a639p
500			_aClassics in Total Synthesis II is the long awaited sequel to Classics in Total Synthesis, a book that has made its mark as a superb tool for educating students and practitioners alike in the art of organic synthesis since its introduction in 1996. In this highly welcomed second volume, K.C. Nicolaou and Scott A. Snyder discuss in detail the most impressive accomplishments in natural product total synthesis during the 1990s and the first years of the 21st century. While all of the features that made the first volume of Classics so popular and unique as a teaching tool have been maintained, in this new treatise the authors seek to present the latest techniques and advance in organic synthesis as they beautifully describe the works of some of the most renowned synthetic organic chemists of our time. complex molecule construction, tin acetal methodology, dithiane nucleophile, enediyne motif, final natural product, vancomycin aglycon, aryl chlorine substituents, heteroaromatic core, synthetic blueprint, enediyne bridge, tetrahydroisoquinoline system, stereochemical elements, aldol stereoselectivity, complex molecule synthesis, oxido bridge, synthetic practitioners, second total synthesis, retrosynthetic analysis, natural product total synthesis, recent total synthesis, stereochemical complexity, olefin metathesis reaction, enyne metathesis,
700			_aSnyder, S. A.
890			_aUK
891			_aScience & Technology - Chemistry {QuickPic}
995			_ANIC _B009932 _CCHM-CHE _D3540.31 _E0 _F049 _G103834 _H0 _I0.00 _J5214.00 32.10% _L20101203 _M2 _UC _W20101216 _XHimanshu Book Co. _ZReference
999			_c15222 _d15222