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1 3) and lactones (30) containing a quaternary asymmetric carbon.
2 (14)N/(15)N isotopomers directly creating an asymmetric carbon.
3  an open-chain amino alcohol cation with two asymmetric carbons.
4 on)contains an iminoribitol cation with four asymmetric carbons.
5  two chiral centers which are defined by two asymmetric carbons.
6         Medicines with a stereogenic center (asymmetric carbon) are mainly present as racemates with
7 iguration regardless of the chirality at the asymmetric carbon atom.
8 inct hydroxyl groups and epimerization of an asymmetric carbon atom.
9 ety attached to a polycyclic framework at an asymmetric carbon atom.
10 ed through the incorporation of a chemically asymmetric carbon atom.
11 letal editing of indoles and pyrroles via an asymmetric carbon-atom insertion, using trifluoromethyl
12 cyclic products with two adjacent quaternary asymmetric carbon atoms, one of which is an all-carbon s
13  lactams alpha-substituted with a quaternary asymmetric carbon bearing a 2-aminophenyl residue.
14 htforward and versatile method for catalytic asymmetric carbon-carbon bond formation at the gamma-pos
15          This methodology represents a novel asymmetric carbon-carbon bond formation between a benzyl
16  The reported methodology represents a novel asymmetric carbon-carbon bond formation in an amino acid
17 ketolase has been employed as a catalyst for asymmetric carbon-carbon bond formation in the synthesis
18 tent with a nickel(0)/nickel(II) pathway for asymmetric carbon-carbon bond formation.
19 ctions as a powerful tool for chemoselective asymmetric carbon-carbon bond formations, including an u
20 heir bioactivity, and the development of new asymmetric carbon-carbon bond-forming reactions.
21     The development of new reactions forming asymmetric carbon-carbon bonds has enabled chemists to s
22                     The presence of a pseudo-asymmetric carbon center provides the motor with unidire
23  generating molecules containing up to three asymmetric carbon centers in just one synthetic step.
24 antly less precedented than the synthesis of asymmetric carbon centers, and strategies for control of
25 c alcohols containing up to three contiguous asymmetric carbon centers.
26 cle, a "clipping" of precession forcing, and asymmetric carbon cycle dynamics, which further enhance
27  challenge is the development of methods for asymmetric carbon-fluorine bond formation from readily a
28                            Carnitine has one asymmetric carbon giving two stereoisomers d and l, but
29                                              Asymmetric carbon-hydrogen (C-H) activation reactions of
30 ted rhodium(III) complex to enable catalytic asymmetric carbon-hydrogen (C-H) activation.
31  The chemical structure of imazalil shows an asymmetric carbon in the C7 position.
32 omer of spirooxindoles with five consecutive asymmetric carbons including spiro and tetrasubstituted
33 sis processes are used to create multi-layer asymmetric carbon molecular sieve (CMS) hollow fiber mem
34                                              Asymmetric carbon molecular sieve (CMS) hollow fiber mem