(EBOOK PDF)Recent Advances in Applications of Name Reactions in Multicomponent Reactions 1st edition by Majid Heravi 9780128196953 0128196955 full chapters

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• ISBN 10:0128196955 

• ISBN 13:9780128196953

• Author:Majid Heravi 

Chapter 1 – Introduction
1.1 – Introduction
1.1.1 – Multicomponent reactions (MCRs)
1.1.2 – General conception
1.1.3 – Green chemistry
1.1.4 – Name reactions
1.2 – Summary and outlook
References
Chapter 2 – Direct synthesis of heterocycles via MCRs, using a name reaction
2.1 – Biginelli reaction
2.2 – Hantzsch reaction
2.3 – Click reaction
2.4 – Gewald reaction
2.5 – Ugi reaction and Ugi-azide reaction
2.5.1 – Ugi-azide reaction
References
Chapter 3 – Synthesis of heterocycles via MCRs, using a name reaction in combination with another re
Anchor 666
3.1 – Michael addition reaction
3.2 – Mannich reaction
3.3 – Aldol reaction
3.4 – Knovenagel reaction
3.5 – Wittig reaction
References
Chapter 4 – Multicomponent reaction via combinations of name reactions
4.1 – Knoevenagel condensation/Michael addition
4.2 – Knoevenagel condensation/Pinner reaction
4.3 – Knoevenagel-type/aza-Diels-Alder
4.4 – Michael addition/Henry reaction
4.5 – Michael type coupling/Knoevenagel reaction
4.6 – Triple-domino Michael/aza-Henry/cyclization reaction
4.7 – Michael addition/Mannich reaction
4.8 – Ugi-4CR/Wittig reaction
4.9 – Ugi/Smiles coupling
4.10 – Ugi-Smiles coupling/intramolecular Diels-Alder cycloaddition
4.11 – Ugi/aza-Wittig reaction
4.12 – Ugi four-component /Povarov-type reaction
4.13 – Joullie-Ugi reaction
4.14 – Click reaction/aldol condensation
4.15 – Knovenagel condensation/click reaction
4.16 – Click reaction/Knoevenagel condensation
4.17 – Sonogashira cross-coupling reaction/Micheal addition
4.18 – Baylis-Hillman/Click reaction
4.19 – Aldol condensation/Michael-type addition
4.20 – Baylis-Hillman type addition/Michael addition
4.21 – Biginelli reactions/Click reaction
4.22 – Micheal addition/Ullman reaction
4.23 – Click reaction/Biginelli reaction
4.24 – Knoevenagel condensation/Hantzsch-like reaction
4.25 – Adol condensation/Michael addition
4.26 – Michael addition/Henry reaction
4.27 – Aldol condensation/Michael addition
4.28 – Aldol condensation/Michael addition
4.29 – Aldol condensation/Michael addition
References
Chapter 5 – Asymmetric multicomponent reactions
5.1 – Introduction
5.2 – Asymmetric Bignelli reaction
5.2.1 – Using chiral catalysts
5.2.2 – Using chiral catalys
5.3 – Asymmetric Ugi reaction
5.4 – Asymmetric Povarov reaction
5.5 – Asymmetric Diels-Alder reaction
5.6 – Asymmetric Mannich reaction
5.7 – Asymmetric Michael addition reaction
5.8 – Asymmetric Aldol reaction
5.9 – Miscellaneous asymmetric reactions
References
Index
Back Cover
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Recent Advances in Applications of Name Reactions in Multicomponent Reactions
Recent Advances in Applications of Name Reactions in Multicomponent Reactions is an ideal reference for researchers and postgraduate students studying organic chemistry, as well as synthetic organic chemists working on the development of novel methodologies for the synthesis of various heterocyclic systems, especially drug design and discovery, in both academia and industry. The book reviews recent applications of name reactions in multicomponents for the synthesis of heterocycles and examines recent advances in applications of significant name reactions, such as Ugi and Passirini, Click, Knoevenagel, Michael, Diels-Alder, Aldol, Mannich, Heck, Huisgen, and Suzuki in MCRs.

These reactions can be used in the synthesis of a wide variety of novel heterocycles with different sizes and heteroatoms, as well as in the total synthesis of natural products in order to decrease the number of synthetic steps. Since chiral inductions are necessary for most of these sequential name reactions, their asymmetric catalyzed reactions are also described.

Includes the synthesis of many heterocycles, which is ideal for synthetic organic chemists engaged in the synthesis of heterocyclic systems
Covers the recent advances of asymmetric synthesis of a wide range of heterocycles in satisfactory enantioselectivities (ees) or distereoselectivities (des)
Reviews the synthesis of a wide variety of interesting heterocycles by using a combination of different and versatile name reactions via MCRs

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