Autor:	Carlos Pérez-Balado, Angel R. de Lera
Rok vydání:	2008
Předmět:	chemistry.chemical_classification Indoles Pyrrolidines Stereochemistry Phenylalanine Organic Chemistry Tryptophan Total synthesis Stereoisomerism Biochemistry Piperazines Indole Alkaloids Amino acid chemistry Physical and Theoretical Chemistry Pyrrolizidine Alkaloids
Zdroj:	Organic Letters. 10:3701-3704
ISSN:	1523-7052 1523-7060
DOI:	10.1021/ol8013073
Popis:	Bispyrrolidinoindoline diketopiperazine alkaloids were synthesized from a common intermediate in seven steps from commercially available amino acids. This versatile synthetic strategy has led to the accomplishment of the first total synthesis of heterodimeric WIN 64745 and a novel approach to homodimeric WIN 64821.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b383f5b765b9474a8b1c123823168983 https://doi.org/10.1021/ol8013073 Zobrazit plný text záznamu