Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Tianzhang, Qiao"'
Autor:
Haigen Fu, Jingzhe Cao, Tianzhang Qiao, Yuyin Qi, Simon J. Charnock, Samuel Garfinkle, Todd K. Hyster
Publikováno v:
Nature
The catalytic asymmetric construction of Csp(3)–Csp(3) bonds remains one of the foremost challenges in organic synthesis.(1) Metal-catalyzed cross-electrophile couplings (XEC) have emerged as a powerful tool for C–C bond formation.(2–5) However
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75470ca26b0ea34d0397116d93e213fe
https://doi.org/10.1038/s41586-022-05167-1
https://doi.org/10.1038/s41586-022-05167-1
Publikováno v:
Synlett. 33:1204-1208
Reductive radical cyclizations are ubiquitous in organic synthesis and have been applied to the synthesis of structurally complex molecules. N-Heterocyclic motifs can be prepared through the cyclization of α-haloamides; however, slow rotation around
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::188da17aba53b976e8e79d82d4e1edcc
https://doi.org/10.1055/s-0040-1719872
https://doi.org/10.1055/s-0040-1719872
Publikováno v:
Journal of the American Chemical Society.
Tertiary nitroalkanes and the corresponding α-tertiary amines represent important motifs in bioactive molecules and natural products. The C-alkylation of secondary nitroalkanes with electrophiles is a straightforward strategy for constructing tertia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d4d5ac25ef376322a7a3108367af71f
http://hdl.handle.net/10261/311028
http://hdl.handle.net/10261/311028
Publikováno v:
Journal of the American Chemical Society.
Tertiary nitroalkanes and the corresponding α-tertiary amines represent important motifs in bioactive molecules and natural products. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d3af76193df40d43c8fdf0f100ef906f
https://pubmed.ncbi.nlm.nih.gov/36608280
https://pubmed.ncbi.nlm.nih.gov/36608280
Tertiary nitroalkanes and the corresponding α-tertiary amines represent important motifs in bioactive molecules and natural prod-ucts. The C-alkylation of secondary nitroalkanes with electrophiles is a straightforward strategy for constructing terti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::feecf8b90f5b240cd93581c6aea477ff
https://doi.org/10.26434/chemrxiv-2022-30n98
https://doi.org/10.26434/chemrxiv-2022-30n98
Autor:
Haigen Fu, Jingzhe Cao, Tianzhang Qiao, Yuyin Qi, Simon Charnock, Samuel Garfinkle, Todd Hyster
The catalytic asymmetric construction of Csp3–Csp3 bonds remains one of the foremost challenges in organic synthesis. Metal-catalyzed cross-electrophile couplings have emerged as a powerful tool for C–C bond formation. However, these catalysts st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7053607e88d05dfde99f7f5a8d5a8781
https://doi.org/10.26434/chemrxiv-2022-38pd0
https://doi.org/10.26434/chemrxiv-2022-38pd0
Autor:
Zhuan Zhang, Michio Sato, Masatoshi Taniguchi, Satoshi Sasamura, Tianzhang Qiao, Man-Cheng Tang, Yui Tamura, Yoshihiro Otsu, Kenji Watanabe, Yi Tang
Publikováno v:
J Am Chem Soc
We report characterization of the biosynthetic pathway of the potent immunosuppressant (-)-FR901483 (1) through heterologous expression and enzymatic assays. The biosynthetic logic to form the azatricyclic alkaloid is consistent with those proposed i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a7dd1d7cb86a3cc3446b525e463a406
https://pubmed.ncbi.nlm.nih.gov/33372776
https://pubmed.ncbi.nlm.nih.gov/33372776
Publikováno v:
Angewandte Chemie (International ed. in English). 59(45)
Phenylfuropyridone natural products from fungi exhibit a range of antibacterial and cytotoxicity activities, and can potentiate azole antifungal compounds. We elucidated the biosynthetic pathway of compounds in the citridone family through heterologo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fdeaf92d44d87f5e3c53e455eab0d5a
https://pubmed.ncbi.nlm.nih.gov/32779306
https://pubmed.ncbi.nlm.nih.gov/32779306