1.
Org Lett
; 26(16): 3327-3331, 2024 Apr 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38160411
RESUMO
The first total synthesis of (-)-merrillianin (1), which is a natural sesquiterpene with a tricyclic structure having a cyclopentane ring and five- and seven-membered lactone parts, is demonstrated. This asymmetric total synthesis enabled the absolute stereostructure determination of naturally occurring (-)-1.
2.
ACS Omega
; 8(30): 27703-27709, 2023 Aug 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37546667
RESUMO
The first total synthesis of (+)-tanzawaic acid B, a natural polyketide bearing a pentadienoic ester and octalin moiety, has been accomplished. The synthetic improvement from previous synthetic conditions facilitated our gram-scale synthesis of the chiral octalin that possesses seven stereogenic centers and that is the core skeleton of almost all of the tanzawaic acid family.
3.
ACS Omega
; 8(33): 30789, 2023 Aug 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37636937
RESUMO
[This corrects the article DOI: 10.1021/acsomega.3c03634.].