Zhanjie Li
Overview
Explore the profile of Zhanjie Li including associated specialties, affiliations and a list of published articles.
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45
Citations
405
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Recent Articles
41.
Li Z, Boyarskikh V, Hansen J, Autschbach J, Musaev D, Davies H
J Am Chem Soc
. 2012 Aug;
134(37):15497-504.
PMID: 22924394
Rhodium-catalyzed reactions of tertiary propargylic alcohols with methyl aryl- and styryldiazoacetates result in tandem reactions, consisting of oxonium ylide formation followed by [2,3]-sigmatropic rearrangement. This process competes favorably with the...
42.
Parr B, Li Z, Davies H
Chem Sci
. 2012 Jun;
2(12):2378-2382.
PMID: 22708053
A domino sequence has been developed between vinyldiazoacetates and racemic allyl alcohols, involving five distinct steps. The sequence generates highly functionalized cyclopentanes with four new stereogenic centers as single diastereomers...
43.
Li Z, Parr B, Davies H
J Am Chem Soc
. 2012 Jun;
134(26):10942-6.
PMID: 22694052
The tandem ylide formation/[2,3]-sigmatropic rearrangement between donor/acceptor rhodium carbenoids and chiral allyl alcohols is a convergent C-C bond forming process, which generates two vicinal stereogenic centers. Any of the four...
44.
Goodman M, Nazarenko A, Casavant B, Li Z, Brennessel W, DeMarco M, et al.
Inorg Chem
. 2012 Jan;
51(2):1084-93.
PMID: 22220571
The new ligand, tris(5-methylpyrazolyl)methane (1), has been prepared by the reaction of n-butyl lithium with tris(pyrazolyl)methane followed by trimethylation of the tetralithiated species with methyl iodide. The BF(4)(-), ClO(4)(-), and...
45.
Li Z, Davies H
J Am Chem Soc
. 2009 Dec;
132(1):396-401.
PMID: 19994854
The rhodium-catalyzed reaction of racemic allyl alcohols with methyl phenyldiazoacetate or methyl styryldiazoacetate results in a two-step process, an initial oxonium ylide formation followed by a [2,3]-sigmatropic rearrangement. This process...