Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Xian-Liang Qi"'
Publikováno v:
Chinese Chemical Letters. 23:661-664
A facile and improved route for the synthesis of the orally active spiroindoline-based growth hormone secretagogue, MK-677 was described. The key step adopted the Fischer indole/reduction strategy. The preparation of the key intermediates N-protected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::608877bf2c0720480b71ce5e49a9d062
https://doi.org/10.1016/j.cclet.2012.03.032
https://doi.org/10.1016/j.cclet.2012.03.032
Publikováno v:
The Journal of Organic Chemistry. 76:3946-3959
An accelerated, enantioselective, and general synthetic route to a class of malyngamides, K (1), L (3), and 5''-epi-C (4), bearing a cyclohexenone ring or a heavily oxygenated six-membered ring and a vinyl chloride structural motif was developed. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bd2ee1dc92c42e1ae17f2329575b568
https://doi.org/10.1021/jo2003852
https://doi.org/10.1021/jo2003852
Publikováno v:
The Journal of Organic Chemistry. 74:4149-4157
A convergent, enantioselective and general synthetic route to a class of marine natural products-malyngamides O (1), P (2), Q (3), R (4), 5''-epi-3 and 5''-epi-4-bearing a novel vinyl chloride structural motif was developed. The key steps involved co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::429cf85ff2d0b31d37f47980cdea5047
https://doi.org/10.1021/jo9003103
https://doi.org/10.1021/jo9003103
Publikováno v:
ChemInform. 43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ad8e17d910cd35d3cd7d739be3dd6a4
https://doi.org/10.1002/chin.201228264
https://doi.org/10.1002/chin.201228264
Publikováno v:
Organicbiomolecular chemistry. 9(10)
A concise enantioselective synthesis of malyngamide W (1) and its 2′-epimer was described. The strategy was based on three key steps: (1) ozonolysis of compound 11 which was derived from (R)-(−)-carvone 8, followed by copper-iron-catalyzed rearra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69c40ff9ad2b66b93f11dad8ccd01632
https://pubmed.ncbi.nlm.nih.gov/21445440
https://pubmed.ncbi.nlm.nih.gov/21445440
Publikováno v:
The Journal of organic chemistry. 73(17)
An accelerated and improved asymmetric synthesis of malyngamide U (1) and its 2'-epimer (2'-epi-1) was accomplished from readily available n-hexanal, ethanolamine and (R)-(-)-carvone. The key steps involved a Johnson-Claisen rearrangement in the synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e96074bd207e36fe6945bae2293ae48
https://pubmed.ncbi.nlm.nih.gov/18656980
https://pubmed.ncbi.nlm.nih.gov/18656980
Publikováno v:
The Journal of Organic Chemistry. 74:7210-7210
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f89e9457a51f6f3021d4262830464ac0
https://doi.org/10.1021/jo901239q
https://doi.org/10.1021/jo901239q
Publikováno v:
Journal of Organic Chemistry; 5/20/2011, Vol. 76 Issue 10, p3946-3959, 14p