Jeżeli nie znalazłeś poszukiwanej książki, skontaktuj się z nami wypełniając formularz kontaktowy.

Ta strona używa plików cookies, by ułatwić korzystanie z serwisu. Mogą Państwo określić warunki przechowywania lub dostępu do plików cookies w swojej przeglądarce zgodnie z polityką prywatności.

Wydawcy

Literatura do programów

Informacje szczegółowe o książce

Named Organic Reactions - ISBN 9780470010419

Named Organic Reactions

ISBN 9780470010419

Autor: Thomas Laue, Andreas Plagens

Wydawca: Wiley

Dostępność: 3-6 tygodni

Cena: 334,95 zł

Przed złożeniem zamówienia prosimy o kontakt mailowy celem potwierdzenia ceny.


ISBN13:      

9780470010419

ISBN10:      

047001041X

Autor:      

Thomas Laue, Andreas Plagens

Oprawa:      

Paperback

Rok Wydania:      

2005-02-18

Numer Wydania:      

2nd Edition

Ilość stron:      

320

Wymiary:      

226x161

Tematy:      

PN

For the Second Edition the authors have completely revised the whole text. With the Baylis–Hillman Reaction and the Swern Oxidation, new reactions have been added. Key reactions such as the Sharpless Epoxidation and the Heck Reaction have been completely revised. Where necessary new references were added and new developments such as the Sharpless Dihydroxylation have been included.
Overall, this book is concentrating on the most important named organic reactions. The reactions are presented in alphabetical order, from the Acyloin Condensation to the Wurtz Reaction. For each reaction clearly outlined reaction mechanisms and applications are presented.
Named Organic Reactions, 2nd Edition providesThe perfect revision aid to key organic reactionsReferences for easy information accessFurther information, including side reactions, yields and variations of the reaction
This book is the essential guide to named organic reactions for chemistry students.

Spis treści:
Introduction to the 2nd Edition.
Acyloin Ester Condensation.
Aldol Reaction.
Alkene Metathesis.
Arbuzov Reaction.
Arndt–Eistert Synthesis.
Baeyer–Villiger Oxidation.
Bamford–Stevens Reaction.
Barton Reaction.
Baylis–Hillman Reaction.
Beckmann Rearrangement.
Benzidine Rearrangement.
Benzilic Acid Rearrangement.
Benzoin Condensation.
Bergman Cyclization.
Birch Reduction.
Blanc Reaction.
Bucherer Reaction.
Cannizzaro Reaction.
Chugaev Reaction.
Claisen Ester Condensation.
Claisen Rearrangement.
Clemmensen Reduction.
Cope Elimination Reaction.
Cope Rearrangement.
Corey–Winter Fragmentation.
Curtius Reaction.
1,3–Dipolar Cycloaddition.
[2Y2 ] Cycloaddition.
Darzens Glycidic Ester Condensation.
Del´epine Reaction.
Diazo Coupling.
Diazotization.
Diels–Alder React ion.
Di–p–Methane Rearrangement.
D¨otz Reaction.
Elbs Reaction.
Ene Reaction.
Ester Pyrolysis.
Favorskii Rearrangement.
Finkelstein Reaction.
Fischer Indole Synthesis.
Friedel–Crafts Acylation.
Friedel–Crafts Alkylation.
Friedl¨ander Quinoline Synthesis.
Fries Rearrangement.
Gabriel Synthesis.
Gattermann Synthesis.
Glaser Coupling Reaction.
Glycol Cleavage.
Gomberg–Bachmann Reaction.
Grignard Reaction.
Haloform Reaction.
Hantzsch Pyridine Synthesis.
Heck Reaction.
Hell–Volhard–Zelinskii Reaction.
Hofmann Elimination Reaction.
Hofmann Rearrangement.
Hunsdiecker Reaction.
Hydroboration.
Japp–Klingemann Reaction.
Knoevenagel Reaction.
Knorr Pyrrole Synthesis.
Kolbe Electrolytic Synthesis.
Kolbe Synthesis of Nitriles.
Kolbe–Schmitt Reaction.
Leuckart–Wallach Reaction.
Lossen Reaction.
Malonic Ester Synthesis.
Mannich Reaction.
McMurry Reaction.
Meerwein–Ponndorf–Verley Reduction.
Michael Reaction.
Mitsunobu Reaction.
Nazarov Cyclization.
Neber Rearrangement.
Nef Reaction.
Norrish Type I Reaction.
Norrish Type II Reaction.
Ozonolysis.
Paterno–B¨uchi Reaction.
Pauson–Khand Reaction.
Perkin Reaction.
Peterson Olefination.
Pinacol Rearrangement.
Prilezhaev Reaction.
Prins Reaction.
Ramberg–B¨acklund Reaction.
Reformatsky Reaction.
Reimer–Tiemann Reaction.
Robinson Annulation.
Rosenmund Reduction.
Sakurai Reaction.
Sandmeyer Reaction.
Schiemann Reaction.
Schmidt Reaction.
Sharpless Epoxidation.
Simmons–Smith Reaction.
Skraup Quinoline Synthesis.
Stevens Rearrangement.
Stille Coupling Reaction.
Stork Enamine Reaction.
Strecker Synthesis.
Suzuki Reaction.
Swern Oxidation.
Tiffeneau–Demjanov Reaction.
Vilsmeier Reaction.
Vinylcyclopr opane Rearrangement.
Wagner–Meerwein Rearrangement.
Weiss Reaction.
Willgerodt Reaction.
Williamson Ether Synthesis.
Wittig Reaction.
Wittig Rearrangement.
Wohl–Ziegler Bromination.
Wolff Rearrangement.
Wolff–Kishner Reduction.
Wurtz Reaction.
Index.

Okładka tylna:
For the Second Edition the authors have completely revised the whole text. With the Baylis–Hillman Reaction and the Swern Oxidation, new reactions have been added. Key reactions such as the Sharpless Epoxidation and the Heck Reaction have been completely revised. Where necessary new references were added and new developments such as the Sharpless Dihydroxylation have been included.
Overall, this book is concentrating on the most important named organic reactions. The reactions are presented in alphabetical order, from the Acyloin Condensation to the Wurtz Reaction. For each reaction clearly outlined reaction mechanisms and applications are presented.
Named Organic Reactions, 2nd Edition providesThe perfect revision aid to key organic reactionsReferences for easy information accessFurther information, including side reactions, yields and variations of the reaction
This book is the essential guide to named organic reactions for chemistry students.

Koszyk

Książek w koszyku: 0 szt.

Wartość zakupów: 0,00 zł

ebooks
covid

Kontakt

Gambit
Centrum Oprogramowania
i Szkoleń Sp. z o.o.

Al. Pokoju 29b/22-24

31-564 Kraków


Siedziba Księgarni

ul. Kordylewskiego 1

31-542 Kraków

+48 12 410 5991

+48 12 410 5987

+48 12 410 5989

Zobacz na mapie google

Wyślij e-mail

Subskrypcje

Administratorem danych osobowych jest firma Gambit COiS Sp. z o.o. Na podany adres będzie wysyłany wyłącznie biuletyn informacyjny.

Autoryzacja płatności

PayU

Informacje na temat autoryzacji płatności poprzez PayU.

PayU banki

© Copyright 2012: GAMBIT COiS Sp. z o.o. Wszelkie prawa zastrzeżone.

Projekt i wykonanie: Alchemia Studio Reklamy