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Catalytic asymmetric organozinc additions to carbonyl compounds
L Pu, HB Yu - Chemical Reviews, 2001 - ACS Publications
Since the initial report of Oguni and Omi on the reaction of diethylzinc with benzaldehyde in
the presence of a catalytic amount of (S)-leucinol with moderate enantioselectivity (49% ee) …
the presence of a catalytic amount of (S)-leucinol with moderate enantioselectivity (49% ee) …
Chiral sulfur ligands for asymmetric catalysis
M Mellah, A Voituriez, E Schulz - Chemical reviews, 2007 - ACS Publications
The preparation of new enantiopure ligands that provide a chiral environment to metals so
that they perform efficient asymmetric catalysis is one of the most straightforward challenges …
that they perform efficient asymmetric catalysis is one of the most straightforward challenges …
Chiral sulfur-containing ligands for asymmetric catalysis
H Pellissier - Tetrahedron, 2007 - Elsevier
The preparation of chiral compounds is an important and challenging area of contemporary
synthetic organic chemistry. 1 In particular, the preparation of new chiral ligands for …
synthetic organic chemistry. 1 In particular, the preparation of new chiral ligands for …
Synthesis of new chiral aliphatic amino diselenides and their application as catalysts for the enantioselective addition of diethylzinc to aldehydes
A set of chiral aliphatic amino diselenides have been synthesized from readily available
starting materials in a straightforward synthetic route via the ring-opening reaction of the …
starting materials in a straightforward synthetic route via the ring-opening reaction of the …
Expeditive synthesis of glycodendrimer scaffolds based on versatile TRIS and mannoside derivatives
YM Chabre, C Contino-Pépin, V Placide… - The Journal of …, 2008 - ACS Publications
A new family of glycodendrimer scaffolds containing 12 and 18 peripheral α-d-
mannopyranosidic units has been synthesized by Cu (I)-catalyzed [1, 3]-dipolar …
mannopyranosidic units has been synthesized by Cu (I)-catalyzed [1, 3]-dipolar …
Asymmetric catalysis with chiral oxazolidine ligands
C Wolf, H Xu - Chemical Communications, 2011 - pubs.rsc.org
Asymmetric catalysis with chiral 1, 3-oxazolidine ligands, which have a sterically tunable,
rigid structure that can accommodate several chiral centers, has found increasing attention …
rigid structure that can accommodate several chiral centers, has found increasing attention …
Chiral diselenide ligands for the asymmetric copper-catalyzed conjugate addition of Grignard reagents to enones
Chiral diselenide ligands for the asymmetric copper-catalyzed conjugate addition of
Grignard reagents to enones - ScienceDirect Skip to main contentSkip to article Elsevier …
Grignard reagents to enones - ScienceDirect Skip to main contentSkip to article Elsevier …
[HTML][HTML] New thioureas based on thiazolidines with antioxidant potential
TL da Silva, LMF Miolo, FSS Sousa, LMP Brod… - Tetrahedron …, 2015 - Elsevier
Thiazolidine and pyrrolidine compounds containing a thiourea moiety were prepared using
boric acid as a coupling agent in a multicomponent methodology. In addition, the antioxidant …
boric acid as a coupling agent in a multicomponent methodology. In addition, the antioxidant …
Thiazolidine-based organocatalysts for a highly enantioselective direct aldol reaction
RS Rambo, PH Schneider - Tetrahedron: Asymmetry, 2010 - Elsevier
A set of enantiopure thiazolidine-based organocatalysts have been synthesized from l-
cysteine, in a straightforward manner allowing numerous structural variations. In particular …
cysteine, in a straightforward manner allowing numerous structural variations. In particular …
Application of N, S-chelating chiral ligands and zinc complexes in catalytic asymmetric hydrosilylation using polymethylhydrosiloxane
S Gérard, Y Pressel, O Riant - Tetrahedron: Asymmetry, 2005 - Elsevier
Application of N,S-chelating chiral ligands and zinc complexes in catalytic asymmetric
hydrosilylation using polymethylhydrosiloxane - ScienceDirect Skip to main contentSkip to …
hydrosilylation using polymethylhydrosiloxane - ScienceDirect Skip to main contentSkip to …