The Experts below are selected from a list of 19140 Experts worldwide ranked by ideXlab platform
Anne Marie Gruber - One of the best experts on this subject based on the ideXlab platform.
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LibGuides. Organic Chemistry Lab - CHEM 2230 - Bumpus. SciFinder Scholar.
2014Co-Authors: Anne Marie GruberAbstract:Guide to locating chemistry research and chemical data. Locating article that use the Named Reaction to synthesize a compound.
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LibGuides: CHEM 2230 - Organic Chemistry Lab - Bumpus: SciFinder Scholar
2014Co-Authors: Anne Marie GruberAbstract:Guide to locating chemistry research and chemical data. Locating article that use the Named Reaction to synthesize a compound.
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LibGuides. Organic Chemistry Lab - CHEM 2230 - Bumpus. Finding Recent Articles.
2014Co-Authors: Anne Marie GruberAbstract:Guide to locating chemistry research and chemical data. Locating article that use the Named Reaction to synthesize a compound.
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LibGuides. SciFinder Scholar. SciFinder Scholar.
2014Co-Authors: Anne Marie GruberAbstract:This guide will allow you to create a SciFinder Scholar account, access SciFinder Scholar, and provide links to SciFinder Scholar training. Locating article that use the Named Reaction to synthesize a compound.
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LibGuides. Organic Chemistry Lab - CHEM 2230 - Manfredi - Thadison. SciFinder Scholar.
2013Co-Authors: Anne Marie Gruber, Chris NeuhausAbstract:A guide to sources for: Named organic Reactions and free radical chlorination. Tips on using SciFinder Scholar and Chemical Abstracts in print. Locating article that use the Named Reaction to synthesize a compound.
Shu-li You - One of the best experts on this subject based on the ideXlab platform.
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Exploring the Chemistry of Spiroindolenines by Mechanistically-Driven Reaction Development: Asymmetric Pictet–Spengler-type Reactions and Beyond
Accounts of chemical research, 2020Co-Authors: Chao Zheng, Shu-li YouAbstract:ConspectusThe Pictet–Spengler Reaction is a fundamental Named Reaction in organic chemistry, and it is the most straightforward method for the synthesis of tetrahydro-β-carbolines, a core structure...
Chao Zheng - One of the best experts on this subject based on the ideXlab platform.
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Exploring the Chemistry of Spiroindolenines by Mechanistically-Driven Reaction Development: Asymmetric Pictet–Spengler-type Reactions and Beyond
Accounts of chemical research, 2020Co-Authors: Chao Zheng, Shu-li YouAbstract:ConspectusThe Pictet–Spengler Reaction is a fundamental Named Reaction in organic chemistry, and it is the most straightforward method for the synthesis of tetrahydro-β-carbolines, a core structure...
Rajender S Varma - One of the best experts on this subject based on the ideXlab platform.
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microwave assisted organic synthesis and transformations using benign Reaction media
Accounts of Chemical Research, 2008Co-Authors: Vivek Polshettiwar, Rajender S VarmaAbstract:A nonclassical heating technique using microwaves, termed "Bunsen burner of the 21st century", is rapidly becoming popular and is dramatically reducing Reaction times. The significant outcomes of microwave (MW)-assisted green chemistry endeavors, which have resulted in the development of synthetic protocols for drugs and fine chemicals synthesis that are relatively more sustainable, are summarized. The use of emerging microwave-assisted chemistry techniques in conjunction with greener Reaction media is dramatically reducing chemical waste and Reaction times in several organic syntheses and chemical transformations. A brief historic account of our own experiences in developing MW-assisted organic transformations, which involve various benign alternatives, such as solid-supported reagents, and greener Reaction media, namely, aqueous, ionic liquid, and solvent-free, for the synthesis of various heterocycles, coupling Reactions, oxidation-reduction Reactions, and some name Reactions are described. Synthesis of Heterocycles. The synthetic chemistry community has been under increased pressure to produce, in an environmentally benign fashion, the myriad of heterocyclic systems required by society in a short span of time, and one of the best options to accelerate these synthetic processes is to use MW technology. The efficient use of the MW heating approach for the synthesis of various heterocyclic compounds in aqueous and solvent-free medium is discussed. Organic Named Reactions. The application of MW chemistry for various Named Reaction such as the Prins Reaction, the Suzuki Reaction, the Heck Reaction, the Aza-Michael Reaction, Trost's gamma-addition, and the Cannizzaro Reaction are summarized. Synthesis and Application of Ionic Liquids. Ionic liquids (ILs), being polar and ionic, in character couple with MW irradiation very efficiently and are, therefore, ideal MW-absorbing candidates for expediting chemical Reactions. MW-assisted solvent-free synthesis and application of ILs are discussed. Oxidation-Reduction Reactions. MW protocols using mineral oxides such as alumina, silica, and clay to immobilize reagents on such solid supports have been extensively explored under "dry" media conditions. Various solvent-free examples of oxidation Reactions are discussed that involve mixing of neat substrates with clay-supported iron(III) nitrate (clayfen) or iodobenzene diacetate (IBD) as an oxidant; some interesting MW reduction protocols using borohydrides are also discussed. Protection-Deprotection Reactions. The protection and deprotection of alcohols and amines are common events in multistep organic syntheses. Various protection and deprotection protocols under MW irradiation are discussed, including tetrahydropyranylation and (benzyloxycarbonyl) (Cbz)-protection, which are the most frequently employed methods.
Chris Neuhaus - One of the best experts on this subject based on the ideXlab platform.
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LibGuides. Organic Chemistry Lab - CHEM 2230 - Manfredi - Thadison. SciFinder Scholar.
2013Co-Authors: Anne Marie Gruber, Chris NeuhausAbstract:A guide to sources for: Named organic Reactions and free radical chlorination. Tips on using SciFinder Scholar and Chemical Abstracts in print. Locating article that use the Named Reaction to synthesize a compound.
