Synthetic applications of furan Diels-Alder chemistry

Autor:	Albert Padwa, C. Oliver Kappe, S. Shaun Murphree
Rok vydání:	1997
Předmět:	Diene Chemistry Organic Chemistry Enantioselective synthesis Substituent Total synthesis Biochemistry Aryne Catalysis chemistry.chemical_compound Intramolecular force Furan Drug Discovery Organic chemistry
Zdroj:	Tetrahedron. 53:14179-14233
ISSN:	0040-4020
DOI:	10.1016/s0040-4020(97)00747-3
Popis:	3. Introduction Bimolecular Diels-Alder Reactions of Furans 2.1. Scope and limitations 2.1.1. Alkenes 2.1.2. Alkynes 2.1.3. Allenes 2.2. Reactive g-bonds 2.3. Catalysts and high pressure 2.4. Asymmetric Diels-Alder reactions 2.5. Total synthesis Intramolecular Diels-Alder Reactions of Furans 3.1. Scope and limitations 3.1.1. Nature of the diene 3.1.1.1. Fused furans 3.1.1.2. Vinyl furans 3.1.2. Nature of the dienophile 3.1.2.1. Alkenes 3.1.2.2. Alkynes 3.1.2.3. Ailenes 3.1.2.4. Benzynes 3.2. Mechanistic considerations 3.2.1. Substituent/structural effects 3.2.2 Catalysts 3.2.3. High-pressure reactions 3.3. Applications 3.3.1. Methodology 3.3.2. Asymmetric synthesis 3.3.3 Synthetic targets
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::a7ed08220f442ca77ea2f8720d56a951 https://doi.org/10.1016/s0040-4020(97)00747-3 Zobrazit plný text záznamu Full Text from ScienceDirect