Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Teega Rammohan Reddy"'
Publikováno v:
RSC Adv.. 4:3149-3152
The synthesis of C1–C8 and C9–C16 fragments of revised structure of (−)-lyngbouilloside is described starting from geraniol and D-malic acid.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d666c89f54e7947fb21ecdaec2889245
https://doi.org/10.1039/c3ra44354j
https://doi.org/10.1039/c3ra44354j
Publikováno v:
Tetrahedron: Asymmetry. 22:2124-2133
The synthesis of gingerol 1 and related compounds 2 – 5 along with diarylheptanoids 6 – 8 has been accomplished using a Keck allylation, Crimmins’ aldol reaction, aldehyde coupling with acetylene, and chelation controlled reductions as the key
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e62d09f666f782687f1a743949989e60
https://doi.org/10.1016/j.tetasy.2011.11.010
https://doi.org/10.1016/j.tetasy.2011.11.010
Publikováno v:
Helvetica Chimica Acta. 94:224-229
The total synthesis of aspinolide A (1) was successfully achieved by an iterative acetyleneepoxide coupling strategy and a Yamaguchi lactonization as the key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd9617a0742aed202d792a7e69947415
https://doi.org/10.1002/hlca.201000161
https://doi.org/10.1002/hlca.201000161
Publikováno v:
Bulletin of the Chemical Society of Japan. 84:229-231
The synthesis of an eight-membered lactone, cephalosporolide D is described using an iterative acetylene–epoxide coupling strategy. The terminal triple bond compound prepared in situ from the known...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::529b57e524f747ccf1cac7ff2a213476
https://doi.org/10.1246/bcsj.20100283
https://doi.org/10.1246/bcsj.20100283
Publikováno v:
ChemInform. 42
Title compound (VI) is synthesized using an iterative acetylene-epoxide coupling [ (III)] and a Yamaguchi lactonization as the key steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36e4db74363d98fdb51cf75b5867873a
https://doi.org/10.1002/chin.201124192
https://doi.org/10.1002/chin.201124192