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More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles, 2 Volume Set
Author: Ana Maria Faisca Phillips
Publisher: John Wiley & Sons
Published: 2022-04-11
Total Pages: 759
ISBN-13: 1119757142
DOWNLOAD EBOOK →More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles An authoritative collection of resources discussing the latest trends in the synthesis of nonaromatic nitrogen heterocycles Widely distributed in nature, nitrogen heterocycles are extremely common in synthetic substances found in pharmaceuticals, agrochemicals, and materials. The literature is evolving rapidly and explores newly emerging structures and medicines. More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles offers R&D professionals the opportunity to easily access a collection of the latest relevant research in the area. In the second two-volume set of this practical reference distinguished researcher Dr. Ana Maria M. M. Faisca Phillips delivers a collection of resources focusing on the newest and most widely applicable trends emerging in synthetic strategies for nonaromatic nitrogen heterocycles. With coverage of topics including organocatalysis, cascade reactions, flow chemistry in synthesis, cycloaddition reactions, metathesis, cross-coupling reactions, and electrochemistry, the book provides quick access to critical new avenues of synthesis. More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles: Volume 1 and 2 also offers readers: A thorough introduction to recent advances in the design and synthesis of cyclic peptidomimetics Comprehensive explorations of fused heterocycles and transition metal promoted synthesis of isoindoline derivatives Practical discussions of 1,4-diazepane ring-based systems and recent advances in the synthesis of azepane-based compounds In-depth examinations of strained aziridinium ions, asymmetric organocatalysis in alternative media, and the electrochemical synthesis of non-aromatic N-heterocycles Perfect for academic and industrial researchers in organic chemistry and synthesis, organometallic chemistry, pharmaceutical chemistry catalysis, and sustainable chemistry, More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles: Volume 1 and 2 is an indispensable reference for anyone seeking an authoritative source of information on new and emerging trends in synthesis.
New Methods for the Asymmetric Synthesis of Nitrogen Containing Heterocycles
Asymmetric Synthesis of Nitrogen Heterocycles
Author: Jacques Royer
Publisher: John Wiley & Sons
Published: 2009-08-04
Total Pages: 425
ISBN-13: 3527625518
DOWNLOAD EBOOK →Here, all aspects of the topic are presented in a compact manner. The book is clearly structured, and divided into two sections -- asymmetric synthesis of heterocycles containing only one nitrogen and that of those with more than one nitrogen as a heteroatom -- such that the necessary information may be found at a glance. The international team of authors provides important experimental procedures, including industrial applications. Essential for synthetic chemists in pharmaceutical and agrochemical chemistry.
More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles, 2 Volume Set
Author: Ana Maria Faisca Phillips
Publisher: John Wiley & Sons
Published: 2022-04-04
Total Pages: 759
ISBN-13: 1119757126
DOWNLOAD EBOOK →More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles An authoritative collection of resources discussing the latest trends in the synthesis of nonaromatic nitrogen heterocycles Widely distributed in nature, nitrogen heterocycles are extremely common in synthetic substances found in pharmaceuticals, agrochemicals, and materials. The literature is evolving rapidly and explores newly emerging structures and medicines. More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles offers R&D professionals the opportunity to easily access a collection of the latest relevant research in the area. In the second two-volume set of this practical reference distinguished researcher Dr. Ana Maria M. M. Faisca Phillips delivers a collection of resources focusing on the newest and most widely applicable trends emerging in synthetic strategies for nonaromatic nitrogen heterocycles. With coverage of topics including organocatalysis, cascade reactions, flow chemistry in synthesis, cycloaddition reactions, metathesis, cross-coupling reactions, and electrochemistry, the book provides quick access to critical new avenues of synthesis. More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles: Volume 1 and 2 also offers readers: A thorough introduction to recent advances in the design and synthesis of cyclic peptidomimetics Comprehensive explorations of fused heterocycles and transition metal promoted synthesis of isoindoline derivatives Practical discussions of 1,4-diazepane ring-based systems and recent advances in the synthesis of azepane-based compounds In-depth examinations of strained aziridinium ions, asymmetric organocatalysis in alternative media, and the electrochemical synthesis of non-aromatic N-heterocycles Perfect for academic and industrial researchers in organic chemistry and synthesis, organometallic chemistry, pharmaceutical chemistry catalysis, and sustainable chemistry, More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles: Volume 1 and 2 is an indispensable reference for anyone seeking an authoritative source of information on new and emerging trends in synthesis.
NEW METHODOLOGIES FOR THE ASYMMETRIC SYNTHESES OF AMINES AND NITROGEN HETEROCYCLES FROM ENANTIOPURE SULFINIMINES (N-SULFINYL IMINES)
Author: HUI Qiu
Publisher:
Published: 2009
Total Pages: 158
ISBN-13:
DOWNLOAD EBOOK →The objective of this research was to development new methodologies for the asymmetric syntheses of amine and natural products from enantiopure sulfinimines (N-sulfinyl imines). In this context, new methods was devised for the asymmetric synthesis of 2,5-cis and trans-disubstituted pyrrolidines from 3-oxo pyrrolidine 2-phosphonates, prepared by an intramolecular metal carbenoid N-H insertion from a sulfinimine derived delta-amino-alpha-diazo- beta-ketophosphonate. Horner-Wadsworth-Emmos reaction of the 3-oxo pyrrolidine 2-phosphonates and aldehydes provided pyrrolidine enones. Hydrogenation (Pd/H2) of the pyrrolidine enones gave cis-2,5-disubstituted pyrrolidines. Luche reduction the pyrrolidine enones followed by a TFA-NaBH3CN mediated hydroxy directed reduction provided the 2,5-trans products. (+)-Preussin, a potent antiviral and antitumor agent was prepared in 9 steps in 28% overall yield from the sulfinimine. An acid catalyzed intramolecular Mannich cyclization of a sulfinimine-derived N-sulfinyl syn-alpha-methyl-beta-amino ketones was employed for the asymmetric synthesis of 2,3,5,6-tetrasubstituted piperidinones. The beta-amino ketones were prepare by treatment of prochiral lithium Weinreb amide enolates with enantiopure (E)-N-(4-(benzyloxy)butylidene)-2,4,6-triisopropylbenzenesulfinamide. This new methodology was highlighted in the first asymmetric synthesis of the poison frog alkaloid (-)-indolizidine 221T. By manipulation of water concentration in tetrahydrofuran, syn- and anti-2,3-diamino esters were prepared by treatment of the lithium enolate of N-(diphenylmethylene) glycine ethyl ester with sulfinimines. Anhydrous THF afforded enantiopure syn-2,3-diamino esters with a syn/anti selectivity of better than 25:1. In a THF-H2O the anti-2,3-diamino esters were formed. The mechanism involves the generation of H2O-LDA species in the formation of enolate which inhibited the retro-Mannich fragmentation in the diamino ester species. (SR,2S,3R)-(-)-Ethyl-2-(N,N-dibenzylamino)-3-N-(p-toluenesulfinyl)amino-pent-4-enoate was employed in an improved total synthesis of the anti-tumor antibiotic (-)-agelastatin A. A series of N-sulfinyl aza-Morita-Baylis-Hillman products were prepared by addition of vinylaluminum and N-methylmorpholine-N-oxide reagents to enantiopure N-(p-toluenesufinyl)- and N-(2-methypropanesulfinyl)-derived sulfinimines from the least hindered direction via a non-chelation control mechanism. Hydrogenation of the these acrylates with a rhodium(I) catalyst afforded anti-alpha-substituted-beta-amino esters with a anti/syn selectivity of better than 17:1. This new methodology is useful for the asymmetric synthesis of anti-alpha-alkyl-beta-amino esters, which are valuable chiral building blocks for the preparation of biologically active nitrogen-containing natural products.
From First Light to Reionization
Author: Massimo S. Stiavelli
Publisher: Wiley-VCH
Published: 2009-06-29
Total Pages: 230
ISBN-13: 9783527627363
DOWNLOAD EBOOK →This up-to-date and concise account of a critical period of the early universe directly links the latest theories and experiments. Targeted at cosmological problems rather than specific methods, it begins with an introduction reviewing the early universe and looks at why reionization is important. The process of reionization analyzes simple analytical considerations and compares existing observations, while a further chapter describes some of the issues regarding the transition from Population III to Population II stars, as well as the constraints that can be derived from WMAP. Further chapters survey the latest numerical modeling and future perspectives for studying the dark ages using galaxies as probes. Written by a scientist with much experience in both research and writing, this account is equally suitable for young researchers as well as master and PhD students.
Synthesis of Naturally Occurring Nitrogen Heterocycles from Carbohydrates
Author: El Sayed H. El Ashry
Publisher: John Wiley & Sons
Published: 2008-04-15
Total Pages: 464
ISBN-13: 1405144793
DOWNLOAD EBOOK →Carbohydrates are widely distributed in nature and widely available, and so are considered as a promising feedstock for the preparation of many organic chemical compounds. They are particularly useful in the preparation of nitrogen heterocycles because of their related structural characteristics and easy availability. Synthesis of Naturally Occurring Nitrogen Heterocycles from Carbohydrates will review the recent literature dealing with use of carbohydrates as raw materials in the synthesis of these materials. The text contains six chapters arranged according to the complexity of the heterocyclic compounds discussed, ranging from five to seven membered rings and from single to multiple fused rings. The book provides a detailed discussion of the various synthetic approaches to these compounds, using carbohydrate starting materials, and does not merely reference synthetic methodology but attempts to give as much detail as possible on the actual experimental conditions used, in such a way that the chemist can use the information directly to design a multi-step synthesis. It discusses the different approaches to the synthesis of a wide range of naturally occurring nitrogen heterocycles in a format that enables the reader to make comparisons and decisions on whether to use a certain procedure, to modify it, or to devise a new synthetic methodology.
Nitrogen Heterocycles in Asymmetric Synthesis
New Methods for the Synthesis of Oxygen and Nitrogen Containing Heterocycles
Author: Matthew Paul Brichacek
Publisher:
Published: 2010
Total Pages: 0
ISBN-13:
DOWNLOAD EBOOK →A single synthetic method rarely is sufficient to provide universal access to a chemical structure class. This realization forces organic chemists to devise and develop new methods. The copper catalyzed ring expansion of vinylaziridines produces nitrogen containing heterocycles commonly found in pharmaceuticals and natural products. This reaction is described from its initial discovery, through optimization, to application. Many substitution patterns and functional groups were tested and the reaction was found to be quite tolerant. By controlling the aziridine and olefin stereochemistry the selective synthesis of either cis or trans 2,5dihydropyrroles was achieved. Likewise, vinyloxiranes were stereoselectively converted to cis- or trans-2,5-dihydrofurans. Furthermore, the asymmetric synthesis of 2-substituted-2,5-dihydrofurans was achieved using chirality transfer characteristic of a [1,3]- sigmatropic rearrangement. This method was further tested by completing the total synthesis of natural products goniothalesdiol and varitriol.
