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Asymmetric synthesis of 3, 3-disubstituted oxindoles

Asymmetric synthesis of 3, 3-disubstituted oxindoles
Asymmetric synthesis of 3, 3-disubstituted oxindoles
Indole derivatives are the most common heterocycle compounds present in nature, for this reason, they have been referred to as ""privileged structures"". In fact, many approved drugs — and natural products — belong to this family. Among indole derivatives, oxindoles have a structural complexity, which have stimulated generations of synthetic chemists to design strategies for assembling these structures, and their enantioselective synthesis is still growing. This book proposes to describe the known enantioselective syntheses of oxindole derivatives. It is divided in six chapters each referring to a specific class of asymmetric oxindole derivatives. After the introduction, Chapter 2 describes all-carbon spirooxindoles; Chapter 3, open-chain 3,3-dialkyloxindoles; Chapter 4, 3-substituted-3-aminooxindoles; Chapter 5, 3-substituted-3-hydroxyoxindoles; Chapter 6, 3-hetero-3-substituted oxindoles. It will be a useful tool for synthetic chemists, who assemble total synthesis of natural products, as well as for drug discovery chemists either in academic or in industry R&S laboratories.
Oxindoles, Synthesis
World Scientific
DalPozzo, Renato
f702d2bb-db42-40dd-952f-9267c381d7a7
Pellissier, Helene
34b041f9-f276-47c6-96c1-d7801d3fe695
Chimni, Swapandeep Singh
3fe53a8d-3150-4ecf-b2d7-8e93bba0c606
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441
DalPozzo, Renato
f702d2bb-db42-40dd-952f-9267c381d7a7
Pellissier, Helene
34b041f9-f276-47c6-96c1-d7801d3fe695
Chimni, Swapandeep Singh
3fe53a8d-3150-4ecf-b2d7-8e93bba0c606
Rios, Ramon
609bedf2-e886-4d62-a676-a32b6f8c1441

DalPozzo, Renato, Pellissier, Helene, Chimni, Swapandeep Singh and Rios, Ramon (2019) Asymmetric synthesis of 3, 3-disubstituted oxindoles , World Scientific, 320pp.

Record type: Book

Abstract

Indole derivatives are the most common heterocycle compounds present in nature, for this reason, they have been referred to as ""privileged structures"". In fact, many approved drugs — and natural products — belong to this family. Among indole derivatives, oxindoles have a structural complexity, which have stimulated generations of synthetic chemists to design strategies for assembling these structures, and their enantioselective synthesis is still growing. This book proposes to describe the known enantioselective syntheses of oxindole derivatives. It is divided in six chapters each referring to a specific class of asymmetric oxindole derivatives. After the introduction, Chapter 2 describes all-carbon spirooxindoles; Chapter 3, open-chain 3,3-dialkyloxindoles; Chapter 4, 3-substituted-3-aminooxindoles; Chapter 5, 3-substituted-3-hydroxyoxindoles; Chapter 6, 3-hetero-3-substituted oxindoles. It will be a useful tool for synthetic chemists, who assemble total synthesis of natural products, as well as for drug discovery chemists either in academic or in industry R&S laboratories.

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More information

Published date: 18 September 2019
Keywords: Oxindoles, Synthesis

Identifiers

Local EPrints ID: 436247
URI: http://eprints.soton.ac.uk/id/eprint/436247
PURE UUID: 5325e0b0-88d6-45f2-9c6b-9ea16e4a39a1
ORCID for Ramon Rios: ORCID iD orcid.org/0000-0002-3843-8521

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Date deposited: 04 Dec 2019 17:30
Last modified: 08 Jan 2024 17:51

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Contributors

Author: Renato DalPozzo
Author: Helene Pellissier
Author: Swapandeep Singh Chimni
Author: Ramon Rios ORCID iD

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