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دانلود کتاب NAME REACTIONS : a collection of detailed mechanisms and synthetic applications.
دانلود کتاب واکنش های نام: مجموعه ای از مکانیسم های دقیق و کاربردهای مصنوعی.
مشخصات کتاب
NAME REACTIONS : a collection of detailed mechanisms and synthetic applications.
ویرایش: 6
نویسندگان: JIE JACK LI
سری:
ISBN (شابک) : 9783030508647, 3030508641
ناشر: SPRINGER NATURE
سال نشر: 2020
تعداد صفحات: 620
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 53 مگابایت
قیمت کتاب (تومان) : 45,000
در صورت تبدیل فایل کتاب NAME REACTIONS : a collection of detailed mechanisms and synthetic applications. به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب واکنش های نام: مجموعه ای از مکانیسم های دقیق و کاربردهای مصنوعی. نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
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فهرست مطالب
Preface Table of Contents Abbreviations and Acronyms Alder Ene Reaction References Aldol Condensation References Arndt–Eistert Homologation References Baeyer–Villiger Oxidation References Baker–Venkataraman Rearrangement References Bamford–Stevens Reaction References Barbier Reaction References Barton–McCombie Deoxygenation References Beckmann Rearrangement References Abnormal Beckmann Rearrangement References Benzilic Acid Rearrangement References Benzoin Condensation References Bergman Cyclization References Biginelli Reaction References Birch Reduction References Bischler–Napieralski Reaction References Brook Rearrangement References Brown Hydroboration References Bucherer–Bergs Reaction References Büchner Ring Expansion References Buchwald–Hartwig Amination References Burgess reagent References Cadiot–Chodkiewicz Coupling References Cannizzaro Reaction References Catellani Reaction References Chan–Lam C–X Coupling Reaction References Chapman Rearrangement References Chichibabin Pyridine Synthesis References Chugaev Elimination References Claisen Condensation References Claisen Rearrangement References para- Claisen Rearrangement References Abnormal Claisen Rearrangement References Eschenmoser–Claisen Amide Acetal Rearrangement References Ireland–Claisen (Silyl Ketene Acetal) Rearrangement References Johnson–Claisen Orthoester Rearrangement References Clemmensen Reduction References Cope Elimination References Cope Rearrangement References Anionic Oxy-Cope Rearrangement References Oxy-Cope Rearrangement References Siloxy-Cope Rearrangement References Corey–Bakshi–Shibata (CBS) Reduction References Corey–Chaykovsky Reaction References Corey–Fuchs Reaction References Curtius Rearrangement References Dakin Oxidation References Dakin–West Reaction References Darzens Condensation References de Mayo Reaction References Demjanov Rearrangement References Tiffeneau–Demjanov Rearrangement References Dess–Martin Periodinane Oxidation References Dieckmann Condensation References Diels–Alder Reaction References Hetero-Diels–Alder Reaction References Inverse-electron-demand Diels–Alder Reaction References Dienone–Phenol Rearrangement References Dötz Reaction References Eschweiler–Clarke Reductive Amination References Favorskii Rearrangement References Quasi-Favorskii Rearrangement Ferrier Carbocyclization References Ferrier Glycal Allylic Rearrangement References Fischer Indole Synthesis References Friedel–Crafts Reaction References Friedel–Crafts Acylation Reaction: Friedel–Crafts Alkylation Reaction: Friedländer Quinoline Synthesis References Fries Rearrangement References Gabriel Synthesis References Ing–Manske Procedure Gewald Aminothiophene Synthesis References Glaser Coupling References Eglinton Coupling References Gould–Jacobs Reaction References Grignard Reaction References Grob Fragmentation References Hajos–Wiechert Reaction References Hantzsch Dihydropyridine Synthesis References Heck Reaction References Henry Nitroaldol Reaction References Hiyama Reaction References Hofmann Elimination References Hofmann Rearrangement References Hofmann–Löffler–Freytag Reaction References Horner–Wadsworth–Emmons Reaction References Still–Gennari Phosphonates References Houben–Hoesch Reaction References Hunsdiecker–Borodin Reaction References Jacobsen–Katsuki Epoxidation References Jones Oxidation Jones Oxidation References Collins Oxidation References PCC Oxidation References PDC Oxidation References Julia–Kocienski Olefination References Julia–Lythgoe Olefination References Knoevenagel Condensation References Knorr Pyrazole Synthesis References Koenig–Knorr Glycosidation References Krapcho Reaction References Kröhnke Pyridine Synthesis References Kumada Reaction References Lawesson's Reagent References Leuckart–Wallach Reaction References Lossen Rearrangement References McMurry Coupling References Mannich Reaction References Markovnikov's Rule References Anti–Markovnikov's Rule References Martin's Sulfurane Dehydrating Reagent References Meerwein–Ponndorf–Verley Reduction References Meisenheimer Complex References Meyer–Schuster Rearrangement References Michael Addition References Michaelis–Arbuzov Phosphonate Synthesis References Minisci Reaction References Mitsunobu Reaction References Miyaura Borylation References Morita–Baylis–Hillman Reaction References Mukaiyama Aldol Reaction References Mukaiyama Michael Addition References Mukaiyama Reagent References Nazarov Cyclization References Neber Rearrangement References Nef Reaction References Negishi Cross-Coupling Reaction References Newman–Kwart Rearrangement References Nicholas Reaction References Noyori Asymmetric Hydrogenation References Nozaki–Hiyama–Kishi Reaction References Olefin Metathesis References Oppenauer Oxidation References Overman Rearrangement References Paal–Knorr Pyrrole Synthesis References Parham Cyclization References Passerini Reaction References Paternó–Büchi Reaction References Pauson–Khand Reaction References Payne Rearrangement References Petasis Reaction References Peterson Olefination References Pictet–Spengler Tetrahydroisoquinoline Synthesis References Pinacol Rearrangement References Pinner Reaction References Polonovski Reaction References Polonovski–Potier Reaction References Prins Reaction References Pummerer Rearrangement References Ramberg–Bäcklund Reaction References Reformatsky Reaction References Ritter Reaction References Robinson Annulation References Sandmeyer Reaction References Schiemann Reaction References Schmidt Rearrangement References Shapiro Reaction References Sharpless Asymmetric Amino-hydroxylation References Sharpless Asymmetric Dihydroxylation References Sharpless Asymmetric Epoxidation References Simmons–Smith Reaction References Smiles Rearrangement References TruceSmile Rearrangement References Sommelet–Hauser Rearrangement References Sonogashira Reaction References Stetter Reaction References Stevens Rearrangement References Stille Coupling References Strecker Amino Acid Synthesis References Suzuki–Miyaura Coupling References Swern Oxidation References Takai Reaction References Tebbe Reagent References Tsuji–Trost Reaction References Ugi Reaction References Ullmann Coupling References Vilsmeier–Haack Reaction References von Braun Reaction References Wacker Oxidation References Wagner–Meerwein Rearrangement References Williamson Ether Synthesis References Wittig Reaction References [1,2]-Wittig Rearrangement References [2,3]-Wittig Rearrangement References Wolff Rearrangement References Wolff–Kishner Reaction References Index
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