Conformational control of nonplanar free base porphyrins: towards bifunctional catalysts of tunable basicity.

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Conformational control of nonplanar free base porphyrins: towards bifunctional catalysts of tunable basicity.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Conformational control of nonp ...... catalysts of tunable basicity.

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Conformational control of nonp ...... catalysts of tunable basicity.

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Conformational control of nonp ...... catalysts of tunable basicity.

@en

Conformational control of nonp ...... catalysts of tunable basicity.

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Conformational control of nonp ...... catalysts of tunable basicity.

@en

Conformational control of nonp ...... catalysts of tunable basicity.

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P1476

Conformational control of nonp ...... catalysts of tunable basicity.

@en

P2093

M Roucan

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S S R Bernhard

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P2860

Chelatases: distort to select?

Porphyrins as Catalysts in Scalable Organic Reactions

Tetrapyrroles: the pigments of life

Enantioselective Michael reaction of malonates to nitroolefins catalyzed by bifunctional organocatalysts.

Highly enantioselective conjugate addition of nitromethane to chalcones using bifunctional cinchona organocatalysts.

Urea- and thiourea-substituted cinchona alkaloid derivatives as highly efficient bifunctional organocatalysts for the asymmetric addition of malonate to nitroalkenes: inversion of configuration at C9 dramatically improves catalyst performance.

N-Methylprotoporphyrin IX: chemical synthesis and identification as the green pigment produced by 3,5-diethoxycarbonyl-1,4-dihydrocollidine treatment

Chiral squaramide derivatives are excellent hydrogen bond donor catalysts.

Influence of electronic and structural effects on the oxidative behavior of nickel porphyrins.

Cinchona Alkaloid-Catalyzed Asymmetric Conjugate Additions: The Bifunctional Brønsted Acid-Hydrogen Bonding Model.

P304

26-29

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scholarly article

P356

10.1039/C7CC08099A

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P407

English

P433

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P478

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P50

Stephen J Connon

Mathias O Senge

Marc Kielmann

P577

2017-12-11T00:00:00Z

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P698

29226923

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