Výsledky vyhledávání - "Shi-Ling Liu"

Novel Stereoselective Syntheses of (+)-Streptol and (−)-1-epi-Streptol Starting from Naturally Abundant (−)-Shikimic Acid

Autor: Yun-Gang He, Wen-Jing Xie, Shi-Ling Liu, Xiao-Xin Shi, Yong-Kang Huang, Xing-Liang Zhu, Yong-Qiang Luo, Lei Wang

Publikováno v: ACS Omega, Vol 6, Iss 26, Pp 17103-17112 (2021)

Novel highly stereoselective syntheses of (+)-streptol and (-)-1-epi-streptol starting from naturally abundant (-)-shikimic acid were described in this article. (-)-Shikimic acid was first converted to the common key intermediate by 11 steps in 40% y

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03f714b0fd0a8bf3e033d958ab2a5aac
https://doi.org/10.1021/acsomega.1c02502

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Efficient and Highly Stereoselective Syntheses of (+)-proto-Quercitol and (−)-gala-Quercitol Starting from the Naturally Abundant (−)-Shikimic Acid

Autor: Feng-Lei Li, Xiao-Xin Shi, Mian-Mian Sun, Lei Wang, Xing-Liang Zhu, Yun-Gang He, Shi-Ling Liu, Yong-Qiang Luo

Publikováno v: ACS Omega, Vol 5, Iss 4, Pp 1813-1821 (2020)
ACS Omega

Efficient and highly stereoselective syntheses of (+)-proto-quercitol and (-)-gala-quercitol starting from the naturally abundant (-)-shikimic acid were described in this article. (-)-Shikimic acid was first converted to the key intermediate by eight

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48ea6255735614c1ea4f2841652e1c35
https://doaj.org/article/e90cc98f9afa4c04a77cbe5720ae24a3

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Novel stereoselective syntheses of N-octyl-β-valienamine (NOV) and N-octyl-4-epi-β-valienamine (NOEV) from (−)-shikimic acid

Autor: Shi-Ling Liu, Yun-Gang He, Xiao-Xin Shi, Wei Ding, Xing-Liang Zhu, Feng-Lei Li, Mian-Mian Sun, Jiang-Ping Yu

Publikováno v: RSC Advances. 9:42077-42084

N-Octyl-β-valienamine (NOV) 1 and N-octyl-4-epi-β-valienamine (NOEV) 2 are potent chemical chaperone drug candidates for the therapy of lysosomal storage disorders. Novel stereoselective syntheses of NOV 1 and NOEV 2 starting from naturally abundan

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4d58b649e08e090ba325ebd6697304f1
https://doi.org/10.1039/c9ra09235h

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Novel Stereoselective Syntheses of (+)-Streptol and (-)-1

Autor: Xing-Liang, Zhu, Yong-Qiang, Luo, Lei, Wang, Yong-Kang, Huang, Yun-Gang, He, Wen-Jing, Xie, Shi-Ling, Liu, Xiao-Xin, Shi

Publikováno v: ACS Omega

Novel highly stereoselective syntheses of (+)-streptol and (−)-1-epi-streptol starting from naturally abundant (−)-shikimic acid were described in this article. (−)-Shikimic acid was first converted to the common key intermediate by 11 steps in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fcbdabfdb7c42c88720b682f8c0be8d5
https://pubmed.ncbi.nlm.nih.gov/34250367

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Efficient and Practical Syntheses of Enantiomerically Pure (S)-(−)-Norcryptostyline I, (S)-(−)-Norcryptostyline II, (R)-(+)-Salsolidine and (S)-(−)-Norlaudanosineviaa Resolution-Racemization Method

Autor: Wei Ding, Shi-Ling Liu, Xiao-Xin Shi, Zhangli Xu, Xia Lu, Rui-Heng Zhu

Publikováno v: Chinese Journal of Chemistry. 32:1039-1048

Four racemic tetrahydroisoquinolines (RS)-(±)-1–4 were prepared from homoveratrylamine via amidation, Bischler-Napieralski reaction and the subsequent reduction. The enantiomerically pure tetrahydroisoquinolines (S)- (−)-norcryptostyline I [(S)-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1b6e67f81e389950172c6cd4dec27205
https://doi.org/10.1002/cjoc.201400471

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