Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Feng-Tao Sheng"'
Publikováno v:
ACS Catalysis. 13:3841-3846
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0da3460da90a1267042a13c29d83a5c3
https://doi.org/10.1021/acscatal.2c06200
https://doi.org/10.1021/acscatal.2c06200
Publikováno v:
Chinese Journal of Chemistry. 40:2151-2160
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ebedb35fc385fce2bd31fd70d363971
https://doi.org/10.1002/cjoc.202200327
https://doi.org/10.1002/cjoc.202200327
Publikováno v:
Journal of the American Chemical Society. 144(47)
Design of ligands in transition-metal catalyzed reactions is challenging, especially in asymmetric transformations. With each step in the catalytic cycle promoted by its privileged ligand and different steps well-connected by dynamic ligand exchange,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d43705cb39f50d15899ec7e2ee358425
https://pubmed.ncbi.nlm.nih.gov/36395247
https://pubmed.ncbi.nlm.nih.gov/36395247
Publikováno v:
Chinese Journal of Chemistry. 38:583-589
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3ac3c2d3cbd50ef72126c891066e58e
https://doi.org/10.1002/cjoc.202000022
https://doi.org/10.1002/cjoc.202000022
Publikováno v:
Organic & Biomolecular Chemistry. 18:5688-5696
A Brønsted acid-catalyzed C3-alkylation of indolizines has been established with different electrophiles such as ortho-hydroxybenzyl alcohols, other precursors of para-quinone methides and ortho-quinone methides, and 2-indolylmethanol as well. By us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71aba04344bd4fd884ccc8cefda50bfe
https://doi.org/10.1039/d0ob01230k
https://doi.org/10.1039/d0ob01230k
Publikováno v:
Organic Chemistry Frontiers. 7:3967-3998
Chiral indole derivatives such as indolines and indolenines are important heterocyclic frameworks which constitute the core structures of many natural products and bioactive molecules. So, intensive attentions from chemists have been paid to the cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c7c63b8d21746c373441aa43cff730a
https://doi.org/10.1039/d0qo01124j
https://doi.org/10.1039/d0qo01124j
Autor:
Wei Tan, Hai-Qing Wang, Feng Shi, Chun Ma, Feng-Tao Sheng, Yu-Chen Zhang, Shuang Deng, Yinchun Jiao
Publikováno v:
Journal of the American Chemical Society. 142(37)
Atroposelective synthesis of axially chiral molecules has attracted substantial attention from chemists because of the importance of such molecules. However, catalytic asymmetric synthesis of axially chiral styrenes or vinyl arenes is underdeveloped
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ac993b62b925087eacfd64e62606a01
https://pubmed.ncbi.nlm.nih.gov/32845127
https://pubmed.ncbi.nlm.nih.gov/32845127
Publikováno v:
Synthesis.
A base-promoted (2+4) annulation of benzofuran-derived azadienes with para-quinone methide derivatives has been established, which afforded spiro-benzofuran derivatives in generally high yields (57–97%) and with good diastereoselectivities (85:15 t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d521ba99efa61cb9e37e9e5f90789da9
https://doi.org/10.1055/s-0040-1707205
https://doi.org/10.1055/s-0040-1707205
Publikováno v:
Angewandte Chemie. 131:3046-3052
The first catalytic asymmetric construction of 3,3'-bisindole skeletons bearing both axial and central chirality has been established by organocatalytic asymmetric addition reactions of 2-substituted 3,3'-bisindoles with 3-indolylmethanols (up to 98
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48db7ce8a196501e13dd727d2db2d73d
https://doi.org/10.1002/ange.201811177
https://doi.org/10.1002/ange.201811177
Publikováno v:
Angewandte Chemie International Edition. 58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4b3b98bfbae460e35c97e4c21d0b725
https://doi.org/10.1002/anie.201981061
https://doi.org/10.1002/anie.201981061