1.
Org Biomol Chem
; 17(8): 2289, 2019 02 20.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30735226
RESUMO
Retraction of 'Organocatalytic stereoselective synthesis of passifloricin A' by Pradeep Kumar et al., Org. Biomol. Chem., 2012, 10, 1820-1825.
2.
Org Biomol Chem
; 10(9): 1820-5, 2012 Mar 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22246108
RESUMO
The enantioselective synthesis of passifloricin A has been achieved in high diastereomeric excess. The 1,3-polyol moiety was constructed by iterative proline-catalyzed sequential α-aminoxylation and Horner-Wadsworth-Emmons (HWE) olefination of aldehydes while the synthesis of lactone moiety was achieved by ring-closing metathesis (RCM).
Assuntos
Pironas/síntese química , Catálise , Estrutura Molecular , Estereoisomerismo
3.
RSC Adv
; 9(6): 3336, 2019 Jan 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35560871
RESUMO
[This retracts the article DOI: 10.1039/C3RA43048K.].