Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Baihua Ye"'
Autor:
Jie Zhao, Son C. Nguyen, Rong Ye, Baihua Ye, Horst Weller, Gábor A. Somorjai, A. Paul Alivisatos, F. Dean Toste
Publikováno v:
ACS Central Science, Vol 3, Iss 5, Pp 482-488 (2017)
Externí odkaz:
https://doaj.org/article/1f98be20c87d4dccbbc0a2d2e23fc670
Publikováno v:
Chem. 9:869-880
Autor:
Fang-Jie Liu, F. Dean Toste, Baihua Ye, Ting-Feng Wu, Yue Fu, Peng Liu, Yue-Jiao Zhang, Jian-Tao Tang
Publikováno v:
Chem
Summary Transition metal-catalyzed cross-electrophile coupling (XEC) is a powerful tool for forging C(sp2)–C(sp2) bonds in biaryl molecules from abundant aromatic halides. While the synthesis of unsymmetrical biaryl compounds through multimetallic
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 26(34)
Publikováno v:
Ye, B; Zhao, J; Zhao, K; McKenna, JM; & Toste, FD. (2018). Chiral Diaryliodonium Phosphate Enables Light Driven Diastereoselective α-C(sp3)-H Acetalization. Journal of the American Chemical Society, 140(26), 8350-8356. doi: 10.1021/jacs.8b05962. UC Berkeley: Retrieved from: http://www.escholarship.org/uc/item/5sq7d8tk
© Copyright 2018 American Chemical Society. C(sp3)-H bond functionalization has emerged as a robust tool enabling rapid construction of molecular complexity from simple building blocks, and the development of asymmetric versions of this reaction cre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b672a8cd8b77655ec1a57ebd94b5f1fb
http://www.escholarship.org/uc/item/5sq7d8tk
http://www.escholarship.org/uc/item/5sq7d8tk
Publikováno v:
Journal of the American Chemical Society. 140(26)
C(sp(3))−H bond functionalization has emerged as a robust tool enabling rapid construction of molecular complexity from simple building blocks, and the development of asymmetric versions of this reaction creates a powerful methodology to access ena
Autor:
Nicolai Cramer, Baihua Ye
Publikováno v:
Synlett. 26:1490-1495
The demand for efficient chiral cyclopentadienyl ligands (Cp-x) has increased significantly in recent years, partly because Cp*Rh(III) species have been developed as powerful catalysts for directed C-H functionalization reactions. However, a lack of
Publikováno v:
CHEMISTRY-A EUROPEAN JOURNAL
Chemistry-A European Journal
Chemistry-A European Journal
Rh(III) -catalyzed directed C-H functionalizations of arylhydroxamates have become a valuable synthetic tool. To date, the regioselectivity of the insertion of the unsaturated acceptor into the common cyclometalated intermediate was dependent solely
Autor:
Nicolai Cramer, Baihua Ye
Publikováno v:
J. Am. Chem. Soc.
The lack of robust and tunable chiral versions of cyclopentadienyl (Cp) ligands hampers progress in the development of catalytic asymmetric versions of a myriad of reactions catalyzed by this ubiquitous ligand. Herein, we describe of a class of chira
Publikováno v:
Angewandte Chemie. 124:10762-10766
Director's cut: The pharmaceutically relevant sulfonamide group is shown to be a competent directing group for [Cp*Rh(OAc)(2)]-catalyzed C-H functionalizations. Reactions of the cyclometalated intermediate with internal alkynes provide access to a wi