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Microbial Proline Racemase–Proline Dehydrogenase Cascade for Efficient Production of d-proline and N-boc-5-hydroxy-l-proline from l-proline
Microbial Proline Racemase–Proline Dehydrogenase Cascade for Efficient Production of d-proline and N-boc-5-hydroxy-l-proline from l-proline
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Microbial Proline Racemase–Proline Dehydrogenase Cascade for Efficient Production of d-proline and N-boc-5-hydroxy-l-proline from l-proline

Zhang, Fanfan ; Xia, Shiwen ; Lin, Hui ; Liu, Jiao ; Huang, Wenxin

Applied biochemistry and biotechnology, 2022-09, Vol.194 (9), p.4135-4146 [Periódico revisado por pares]

New York: Springer US

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2
Construction of Challenging Proline–Proline Junctions via Diselenide–Selenoester Ligation Chemistry
Construction of Challenging Proline–Proline Junctions via Diselenide–Selenoester Ligation Chemistry
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Construction of Challenging Proline–Proline Junctions via Diselenide–Selenoester Ligation Chemistry

Sayers, Jessica ; Karpati, Phillip M. T ; Mitchell, Nicholas J ; Goldys, Anna M ; Kwong, Stephen M ; Firth, Neville ; Chan, Bun ; Payne, Richard J

Journal of the American Chemical Society, 2018-10, Vol.140 (41), p.13327-13334 [Periódico revisado por pares]

United States: American Chemical Society

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3
Regio- and Stereospecific Synthesis of C‑3 Functionalized Proline Derivatives by Palladium Catalyzed Directed C(sp3)–H Arylation
Regio- and Stereospecific Synthesis of C‑3 Functionalized Proline Derivatives by Palladium Catalyzed Directed C(sp3)–H Arylation
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Regio- and Stereospecific Synthesis of C‑3 Functionalized Proline Derivatives by Palladium Catalyzed Directed C(sp3)–H Arylation

Affron, Dominic P ; Davis, Owen A ; Bull, James A

Organic letters, 2014-09, Vol.16 (18), p.4956-4959 [Periódico revisado por pares]

United States: American Chemical Society

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4
Proline Editing: A General and Practical Approach to the Synthesis of Functionally and Structurally Diverse Peptides. Analysis of Steric versus Stereoelectronic Effects of 4‑Substituted Prolines on Conformation within Peptides
Proline Editing: A General and Practical Approach to the Synthesis of Functionally and Structurally Diverse Peptides. Analysis of Steric versus Stereoelectronic Effects of 4‑Substituted Prolines on Conformation within Peptides
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Proline Editing: A General and Practical Approach to the Synthesis of Functionally and Structurally Diverse Peptides. Analysis of Steric versus Stereoelectronic Effects of 4‑Substituted Prolines on Conformation within Peptides

Pandey, Anil K ; Naduthambi, Devan ; Thomas, Krista M ; Zondlo, Neal J

Journal of the American Chemical Society, 2013-03, Vol.135 (11), p.4333-4363 [Periódico revisado por pares]

United States: American Chemical Society

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5
Proline: the distribution, frequency, positioning, and common functional roles of proline and polyproline sequences in the human proteome
Proline: the distribution, frequency, positioning, and common functional roles of proline and polyproline sequences in the human proteome
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Proline: the distribution, frequency, positioning, and common functional roles of proline and polyproline sequences in the human proteome

Morgan, Alexander A ; Rubenstein, Edward Casarini, Dulce Elena

PloS one, 2013-01, Vol.8 (1), p.e53785-e53785 [Periódico revisado por pares]

United States: Public Library of Science

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6
Structure-affinity relationships of reversible proline analog inhibitors targeting proline dehydrogenase
Structure-affinity relationships of reversible proline analog inhibitors targeting proline dehydrogenase
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Structure-affinity relationships of reversible proline analog inhibitors targeting proline dehydrogenase

Bogner, Alexandra N ; Tanner, John J

Organic & biomolecular chemistry, 2022-01, Vol.2 (4), p.895-95 [Periódico revisado por pares]

England: Royal Society of Chemistry

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7
An Efficient Synthesis of Pyrrolo[2,3,4-kl]acridin-1-one Derivatives Catalyzed by l‑Proline
An Efficient Synthesis of Pyrrolo[2,3,4-kl]acridin-1-one Derivatives Catalyzed by l‑Proline
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An Efficient Synthesis of Pyrrolo[2,3,4-kl]acridin-1-one Derivatives Catalyzed by l‑Proline

Wang, Huiyuan ; Li, Lili ; Lin, Wei ; Xu, Pan ; Huang, Zhibin ; Shi, Daqing

Organic letters, 2012-09, Vol.14 (17), p.4598-4601 [Periódico revisado por pares]

United States: American Chemical Society

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8
Improving the Catalytic Performance of (S)‑Proline as Organocatalyst in Asymmetric Aldol Reactions in the Presence of Solvate Ionic Liquids: Involvement of a Supramolecular Aggregate
Improving the Catalytic Performance of (S)‑Proline as Organocatalyst in Asymmetric Aldol Reactions in the Presence of Solvate Ionic Liquids: Involvement of a Supramolecular Aggregate
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Improving the Catalytic Performance of (S)‑Proline as Organocatalyst in Asymmetric Aldol Reactions in the Presence of Solvate Ionic Liquids: Involvement of a Supramolecular Aggregate

Obregón-Zúñiga, Arturo ; Milán, Mario ; Juaristi, Eusebio

Organic letters, 2017-03, Vol.19 (5), p.1108-1111 [Periódico revisado por pares]

United States: American Chemical Society

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9
Exogenous Melatonin Counteracts NaCl-Induced Damage by Regulating the Antioxidant System, Proline and Carbohydrates Metabolism in Tomato Seedlings
Exogenous Melatonin Counteracts NaCl-Induced Damage by Regulating the Antioxidant System, Proline and Carbohydrates Metabolism in Tomato Seedlings
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Exogenous Melatonin Counteracts NaCl-Induced Damage by Regulating the Antioxidant System, Proline and Carbohydrates Metabolism in Tomato Seedlings

Siddiqui, Manzer H ; Alamri, Saud ; Al-Khaishany, Mutahhar Y ; Khan, M Nasir ; Al-Amri, Abdullah ; Ali, Hayssam M ; Alaraidh, Ibrahim A ; Alsahli, Abdulaziz A

International journal of molecular sciences, 2019-01, Vol.20 (2), p.353 [Periódico revisado por pares]

Switzerland: MDPI AG

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10
A novel ( S)-proline-modified task-specific chiral ionic liquid—an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water
A novel ( S)-proline-modified task-specific chiral ionic liquid—an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water
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A novel ( S)-proline-modified task-specific chiral ionic liquid—an amphiphilic recoverable catalyst for direct asymmetric aldol reactions in water

Siyutkin, Dmitriy E. ; Kucherenko, Alexander S. ; Struchkova, Marina I. ; Zlotin, Sergei G.

Tetrahedron letters, 2008-02, Vol.49 (7), p.1212-1216 [Periódico revisado por pares]

Elsevier Ltd

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