a-Tertiary Amines en Route to Natural Products (eBook)

Mariya Al-Rashida, Abdul Hameed, Muhammad Raza Shah (Autoren)

eBook Download: EPUB

2021 | 1. Auflage
240 Seiten
Elsevier Science (Verlag)
9780128233689 (ISBN)

Infos

?-Tertiary Amines en Route to Natural Products presents the multistep synthesis of natural products using schematic diagrams. This approach provides a quick-and-easy way to review and understand new and novel synthetic strategies to construct structural frameworks of natural products. The book covers the class of natural products bearing the ?,?-disubstituted ?-amino acid motif. Featured natural product molecules include Altemicidin, Amathaspiramide (A-F), Kaitocephalin, Lactacystin, Salinosporamide, Manzacidins (A,C), Neooxazolomycin, Sphingofungins (E,F), (1S,3R)-1-Aminocyclopentane-1,3-diarboxylic Acid (ACPD), Total synthesis of cephalotaxine and related molecules, ?-amino acids based natural products, ? amino acid based natural products and Tetrodotoxin. This book is ideal for chemists working in the area of organic synthesis, especially those who are involved in the development of new, efficient and novel methodologies for natural product synthesis. - Outlines synthetic strategies for natural products bearing ?-tertiary amines and ?,?-disubstituted ?-amino acid motif - Describes multistep synthetic routes that highlight key steps - Covers asymmetric and diastereoselective synthetic approaches towards targeted natural products - Illustrates multistep synthetic routes related to -amino acids based natural products and -amino acids based natural products

Dr. Abdul Hameed Dr. Abdul Hameed completed his PhD in Organic Chemistry from The University of Nottingham, UK. He worked in the area of natural products synthesis. He was a post-doc fellow in Max-Planck Institut für Polymerforschung, Germany in synthetic division headed by Prof. Dr. Klaus Müllen. There he worked on the functionalization of adenylyl cyclsase inhibitors via chemical methods to conjugate them with monoclonal antibody to study their biological potential in Regulatory T cells (Treg). His current research interests are including the development of novel methodologies, their utilization in natural products synthesis, the synthesis heterocyclic compound compounds to evaluate their biological potential.

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a-Tertiary Amines en Route to Natural Products presents the multistep synthesis of natural products using schematic diagrams. This approach provides a quick-and-easy way to review and understand new and novel synthetic strategies to construct structural frameworks of natural products. The book covers the class of natural products bearing the a,a-disubstituted a-amino acid motif. Featured natural product molecules include Altemicidin, Amathaspiramide (A-F), Kaitocephalin, Lactacystin, Salinosporamide, Manzacidins (A,C), Neooxazolomycin, Sphingofungins (E,F), (1S,3R)-1-Aminocyclopentane-1,3-diarboxylic Acid (ACPD), Total synthesis of cephalotaxine and related molecules, a-amino acids based natural products, a amino acid based natural products and Tetrodotoxin. This book is ideal for chemists working in the area of organic synthesis, especially those who are involved in the development of new, efficient and novel methodologies for natural product synthesis. - Outlines synthetic strategies for natural products bearing a-tertiary amines and a,a-disubstituted a-amino acid motif- Describes multistep synthetic routes that highlight key steps- Covers asymmetric and diastereoselective synthetic approaches towards targeted natural products- Illustrates multistep synthetic routes related to -amino acids based natural products and -amino acids based natural products

Produkt-Details

• Erscheint lt. Verlag: 14.1.2021
• Sprache: englisch
• Themenwelt: Naturwissenschaften ► Chemie ► Organische Chemie
• ISBN-13: 9780128233689 / 9780128233689