Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sie-Mun Lo"'
Autor:
Zhiyuan Ma, Feng Ni, Grace H. C. Woo, Sie-Mun Lo, Philip M. Roveto, Scott E. Schaus, John K. Snyder
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 829-840 (2012)
Intramolecular inverse electron demand cycloadditions of isatin-derived 1,2,4-triazines with acetylenic dienophiles tethered by amidations or transesterifications proceed in excellent yields to produce lactam- or lactone-fused α-carbolines. Beginnin
Externí odkaz:
https://doaj.org/article/009ed6ec6b87448790ef1d3d367869c9
Publikováno v:
The Journal of Organic Chemistry. 69:7171-7182
The intramolecular inverse-electron-demand Diels-Alder reaction between imidazoles and 1,2,4-triazines linked by a trimethylene tether from the imidazole N1 position to the triazine C3 proceed in excellent yields to produce 1,2,3,4-tetrahydro-1,5-nap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b3aeec42eaccded343802e22f66306a
https://doi.org/10.1021/jo040193z
https://doi.org/10.1021/jo040193z
Autor:
Jean E. Lachowicz, Robert E. West, Joyce J. Hwa, Zhiwei Yang, Sie-Mun Lo, Gerald W. Shipps, Shuqin Zheng, Dinesh P. Sinha, Craig R. Mahon, Mark E. Cartwright, Yongqi Deng, Margaret van Heek, Alan S. Bass, Constance Farley
Publikováno v:
Bioorganicmedicinal chemistry letters. 23(3)
Inhibitors based on a benzo-fused spirocyclic oxazepine scaffold were discovered for stearoyl-coenzyme A (CoA) desaturase 1 (SCD1) and subsequently optimized to potent compounds with favorable pharmacokinetic profiles and in vivo efficacy in reducing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fb92f747284357ad52302c1c92fb2a4
https://pubmed.ncbi.nlm.nih.gov/23265904
https://pubmed.ncbi.nlm.nih.gov/23265904
Autor:
Feng Ni, John K. Snyder, Philip Roveto, Zhiyuan Ma, Scott E. Schaus, Grace H. C. Woo, Sie-Mun Lo
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 829-840 (2012)
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 829-840 (2012)
Intramolecular inverse electron demand cycloadditions of isatin-derived 1,2,4-triazines with acetylenic dienophiles tethered by amidations or transesterifications proceed in excellent yields to produce lactam- or lactone-fused α-carbolines. Beginnin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a33007faf575334808a62637212f167a
https://pubmed.ncbi.nlm.nih.gov/23015831
https://pubmed.ncbi.nlm.nih.gov/23015831
Publikováno v:
Journal of Organic Chemistry; 10/15/2004, Vol. 69 Issue 21, p7171-7182, 12p