Enantiodivergent Steglich rearrangement of O-carboxylazlactones catalyzed by a chirality switchable helicene containing a 4-aminopyridine unit.
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A complementary pair of enantioselective switchable organocatalysts.Gold(I)-Catalysed Asymmetric Hydroamination of Alkenes: A Silver- and Solvent-Dependent Enantiodivergent Reaction.Real-Time Control of the Enantioselectivity of a Supramolecular Catalyst Allows Selecting the Configuration of Consecutively Formed Stereogenic Centers.
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Enantiodivergent Steglich rearrangement of O-carboxylazlactones catalyzed by a chirality switchable helicene containing a 4-aminopyridine unit.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 25 August 2016
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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Enantiodivergent Steglich rear ...... aining a 4-aminopyridine unit.
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Enantiodivergent Steglich rear ...... aining a 4-aminopyridine unit.
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Enantiodivergent Steglich rear ...... aining a 4-aminopyridine unit.
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Enantiodivergent Steglich rear ...... aining a 4-aminopyridine unit.
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Enantiodivergent Steglich rear ...... aining a 4-aminopyridine unit.
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Enantiodivergent Steglich rear ...... aining a 4-aminopyridine unit.
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P2860
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Enantiodivergent Steglich rear ...... aining a 4-aminopyridine unit.
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Cheng-Che Tsai
Chien-Tien Chen
Chin-Hui Yu
Gou-Tao Huang
Pei-Kang Tsou
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P304
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10.1039/C6SC02646J
P577
2016-08-25T00:00:00Z