Download E-books Strategic Applications of Named Reactions in Organic Synthesis PDF

Kurti and Czako have produced an crucial instrument for experts and non-specialists in natural chemistry. This leading edge reference paintings comprises 250 natural reactions and their strategic use within the synthesis of complicated typical and unnatural items. Reactions are completely mentioned in a handy, two-page layout--using complete colour. Its accomplished insurance, great association, caliber of presentation, and wealth of references, make this a need for each natural chemist.

* the 1st reference paintings on named reactions to give coloured schemes for less complicated understanding
* 250 often used named reactions are offered in a handy two-page structure with quite a few examples
* a gap checklist of abbreviations contains either constructions and chemical names
* comprises greater than 10,000 references grouped through seminal papers, studies, ameliorations, and theoretical works
* Appendices checklist reactions so as of discovery, team through modern utilization, and supply extra research tools
* large index speedy locates info utilizing phrases present in textual content and drawings

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330 Paterno-Büchi response ...................................................................................................................................... 332 Pauson-Khand response ..................................................................................................................................... 334 xlix TABLE OF CONTENTS seek textual content Payne Rearrangement ........................................................................................................................................ 336 Perkin Reaction................................................................................................................................................... 338 Petasis Boronic Acid-Mannich response ............................................................................................................. 340 Petasis-Ferrier Rearrangement........................................................................................................................... 342 Peterson Olefination............................................................................................................................................ 344 Pfitzner-Moffatt Oxidation.................................................................................................................................... 346 Pictet-Spengler Tetrahydroisoquinoline Synthesis .............................................................................................. 348 Pinacol and Semipinacol Rearrangement ........................................................................................................... 350 Pinner Reaction................................................................................................................................................... 352 Pinnick Oxidation ................................................................................................................................................ 354 Polonovski Reaction............................................................................................................................................ 356 Pomeranz-Fritsch Reaction................................................................................................................................. 358 Prévost Reaction................................................................................................................................................. 360 Prilezhaev response ............................................................................................................................................ 362 Prins Reaction..................................................................................................................................................... 364 Prins-Pinacol Rearrangement ............................................................................................................................. 366 Pummerer Rearrangement .................................................................................................................................

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