Decaspirones and palmarumycins from Phaeoseptum sp. KT4106: Chirality reinvestigation of palmarumycins CP4a and CP5

Autor:	Takeshi Okamura, Kota Inose, Kazuaki Tanaka, Ayane Hayasaka, Satomi Miura, Masaru Hashimoto, Ryuhi Kanehara
Rok vydání:	2021
Předmět:	010405 organic chemistry Stereochemistry Chemistry Organic Chemistry Drug Discovery 010402 general chemistry Chirality (chemistry) 01 natural sciences Biochemistry 0104 chemical sciences
Zdroj:	Tetrahedron. 92:132251
ISSN:	0040-4020
DOI:	10.1016/j.tet.2021.132251
Popis:	5-Dehydrodecaspirones F (1) and H (2) were isolated from Phaeoseptum sp. KT4106 along with known structurally related compounds involving palmarumycins CP4a (3) and CP5 (4). Although these were reported to be pseudo-enantiomers, our chirality reinvestigation found that both possess (2S)-configuration.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::3a5ce60d9c6d9d1e4deb45233de3c276 https://doi.org/10.1016/j.tet.2021.132251 Zobrazit plný text záznamu Full Text from ScienceDirect