Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Laksamee Jeanmard"'
Autor:
Jiraporn Panprasert, Vatcharin Rukachaisirikul, Kwanruthai Tadpetch, Laksamee Jeanmard, Panata Iawsipo
Publikováno v:
Tetrahedron. 74:4521-4529
The first and convergent total syntheses of polyketide natural products dechlorogreensporones A and D have been accomplished in 17 longest linear steps with 2.8% and 5.4% overall yields, respectively, starting from known methyl 2-(2-formyl-3,5-dihydr
Publikováno v:
Tetrahedron Letters. 58:3453-3456
The first total synthesis of greensporone C, a cytotoxic 14-membered resorcylic acid lactone, has been accomplished via a longest linear sequence of 16 steps in 3.3% overall yield. The key features of the synthesis include Mitsunobu esterification an
Publikováno v:
Tetrahedron: Asymmetry. 26:918-923
A chiron approach to the synthesis of the proposed structure of pestalotioprolide A, a 14-membered unsaturated macrolide isolated from the mangrove-derived fungus Pestalotiopsis sp. PSU-MA119, starting from d -(+)-gluconic acid δ-lactone is describe
Autor:
Vatcharin Rukachaisirikul, Laksamee Jeanmard, Souwalak Phongpaichit, Kwanruthai Tadpetch, Aticha Thiraporn, Jariya Sakayaroj, Chatsuda Chukong
Publikováno v:
Phytochemistry Letters. 11:106-110
A new naphthoquinone, solaninaphthoquione (1), and a new succinate ester derivative, 4-(4-hydroxyphenethoxy)-4-oxobutanoic acid (2), were isolated from the soil fungus Fusarium solani PSU-RSPG227 together with five previously reported compounds; java
Publikováno v:
ChemInform. 47
An asymmetric total synthesis of (I) is performed starting from D-(+)-gluconic acid δ-lactone via Yamaguchi esterification and ring-closing metathesis as the key steps.