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List of organic reactions - Wikipedia

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Encyclopedia of Reagents for Organic Synthesis (e-EROS) List of

Bromination is one of the most important transformations in organic synthesis and can be carried out using bromine and many other bromo compounds. Use of molecular bromine in organic synthesis is well-known. However, due to the hazardous nature of bromine, enormous growth has been witnessed in the past several decades for the development of solid bromine carriers. This review outlines the use of bromine and different bromo-organic compounds in organic synthesis. The applications of bromine, a total of 107 bromo-organic compounds, 11 other brominating agents, and a few natural bromine sources were incorporated. The scope of these reagents for various organic transformations such as bromination, cohalogenation, oxidation, cyclization, ring-opening reactions, substitution, rearrangement, hydrolysis, catalysis, etc. has been described briefly to highlight important aspects of the bromo-organic compounds in organic synthesis.

Purchase Strategic Applications of Named Reactions in Organic Synthesis - 1st Edition

The use of such enolate anions from carbonyl compounds is fundamental to organic synthesis and you will already have met them as intermediates in the Aldol reaction and Claisen condensation.

List of computer-assisted organic synthesis software

The online version of Organic Syntheses Based on Name Reactions by A ..

Indranirekha Saikia was born in, Jorhat, Assam, India, in 1983. In 2004, she graduated from J. B. College, Dibrugarh University, majoring in chemistry, and received her master’s degree in 2006 from the same university with specialization in organic chemistry. She obtained her Ph.D. degree in organic chemistry from Gauhati University under the supervision of Dr. Prodeep Phukan in 2012. The main focus of her work is developing new synthetic routes using bromo-organic compounds. At present, Dr. Saikia is working as a Council of Scientific and Industrial Research (CSIR) research associate at the North East Institute of Science and Technology (NEIST), Branch Laboratory, Itanagar, Naharlagun, Arunachal Pradesh, India.

Here is a list of many named reactions. The detailed mechanism is provided for each of them and several samples are given to illustrate their synthetic usefulness.

Hantzsch pyridine synthesis, ..

Browse and Read Organic Chemistry Synthesis Reactions List Organic Chemistry Synthesis Reactions List The ultimate sales letter will provide you a …

Ramakrishnan 7.1 Introduction 203 7.2 Linear, Dendritic, and Hyperbranched Polymers 205 7.3 Telechelic and Block Copolymers 220 7.4 Star and Star-Block Polymers 226 7.5 Cyclic Polymers 230 7.6 Side-Chain Clickable Polymers 235 7.7 Cross-linked Polymeric Systems 238 7.8 Porous Organic Polymers 242 7.9 Surface Modification using CuAAC Reaction 244 7.10 Strain-Promoted Click Reaction 247 7.11 Topochemical Azide-Alkyne Cycloaddition (TAAC) Reactions 249 7.12 Summary and Outlook 251 References 251 8 Thiol-Based "Click" Chemistry for Macromolecular Architecture Design 255Weidong Zhang, Kui Chen, and Gaojian Chen 8.1 Introduction 255 8.2 Thiol Chemistry for Macromolecular Architecture Design 256 8.2.1 Linear Polymers 256 8.2.2 Graft and Comb Polymers 258 8.2.3 Star Polymers 261 8.2.4 Cyclic Polymers 263 8.2.5 Dendritic and Hyperbranched Polymers 265 8.2.6 Conjugated and Hybrid Polymers 270 8.3 Conclusion 276 Acknowledgments 284 References 284 9 Synthesis of Macrocycles and Click Chemistry 287Dario Pasini 9.1 Introduction 287 9.1.1 Peptide- and Sugar-Containing Click Macrocycles 289 9.1.2 Click Macrocycles for Anion Binding and Supramolecular Recognition 297 9.1.3 Clicking Macrocycles to form Mechanical Bonds 300 9.1.4 Cyclic Polymers Obtained by the CuAAC Click Reaction 302 9.2 Summary and Conclusions 304 References 304 10 Modifications of Nucleosides, Nucleotides, and Nucleic Acids using Huisgen's [3+2] Azide-Alkyne Cycloaddition: Opening Pandora's Box 309Franck Amblard, Ozkan Sari, Sebastien Boucle, Ahmed Khalil, and Raymond F.

The sheer number of reactions covered in an undergraduate organic chemistry course can be overwhelming. Students are expected to demonstrate a thorough knowledge of these reactions in order to understand the logic of organic synthesis. A method that allows students to systematically solve organic synthesis problems without memorizing dozens of reactions would be beneficial. Two new card games, Synthesis and Synthetic Dominos, have been developed using a variation of traditional flash cards. Both of these games allow players to develop the logical skills needed to solve organic synthesis problems, review organic functional groups, and review reaction reagents. The first game, Synthesis, is a solitaire game that uses reaction cards to link up a starting material and target by connecting functional group conversions. The game play mimics the process used to solve synthesis problems. The second game, Synthetic Dominos, is a single-player or multiplayer game that has a gameplay similar to that of Dominos. An initial functional group card is dealt, and then players play their cards to build off this initial card. Strings of functional group conversions develop as the game progresses. These games are an excellent method of developing the logic for solving synthesis problems and reviewing organic reactions. These games are especially effective in lower-division organic chemistry courses, upper-division organic synthesis courses, and preparing for placement exams, such as the MCAT and ACS.

Here is a list of many named reactions. The detailed mechanism is provided for each of them and several samples are given to illustrate their synthetic usefulness.
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