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1
Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides
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Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides

Köring, Laura ; Sitte, Nikolai A. ; Paradies, Jan

Synthesis (Stuttgart), 2022-03, Vol.54 (5), p.1287-1300 [Periódico revisado por pares]

Rüdigerstraße 14, 70469 Stuttgart, Germany: Georg Thieme Verlag KG

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Stable and Reusable Binaphthyl-Supported Palladium Catalyst for Aminocarbonylation of Aryl Iodides
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Stable and Reusable Binaphthyl-Supported Palladium Catalyst for Aminocarbonylation of Aryl Iodides

Sharma, Nidhi ; Sekar, Govindasamy

Advanced synthesis & catalysis, 2016-01, Vol.358 (2), p.314-320 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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Radical-Mediated γ-Functionalizations of α,β-Unsaturated Carboxylic Amides
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Radical-Mediated γ-Functionalizations of α,β-Unsaturated Carboxylic Amides

Kim, Sunggak ; Lim, Chae Jo

Angewandte Chemie (International ed.), 2004-10, Vol.43 (40), p.5378-5380 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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4
Nanomicelle drug with acid-triggered doxorubicin release and enhanced cellular uptake ability based on mPEG-graft-poly(N-(2-aminoethyl)-L-aspartamide)-hexahydrophthalic acid copolymers
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Nanomicelle drug with acid-triggered doxorubicin release and enhanced cellular uptake ability based on mPEG-graft-poly(N-(2-aminoethyl)-L-aspartamide)-hexahydrophthalic acid copolymers

Cao, Li ; Xiao, Yi ; Lu, Wei ; Liu, Shiyuan ; Gan, Lin ; Yu, Jiahui ; Huang, Jin

Journal of biomaterials applications, 2018-01, Vol.32 (6), p.826-838 [Periódico revisado por pares]

London, England: SAGE Publications

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5
ChemInform Abstract: Metal‐Catalyzed Formal Amidation of Alkenes under CO‐Free Condition
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ChemInform Abstract: Metal‐Catalyzed Formal Amidation of Alkenes under CO‐Free Condition

Zhang, Yuanyuan ; Ye, Wenjing ; Leng, Xue ; He, Ying ; Zhang, Hui ; Xiao, Xiao

ChemInform, 2016-12, Vol.47 (52), p.no-no

Weinheim: WILEY‐VCH Verlag

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6
ChemInform Abstract: SeO2 Mediated Efficient Synthesis of Amides and α‐Ketoamides of Secondary Amines with Wide Substrate Scope
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ChemInform Abstract: SeO2 Mediated Efficient Synthesis of Amides and α‐Ketoamides of Secondary Amines with Wide Substrate Scope

Meena, Samdarshi ; Singh, Rohit ; Vishwakarma, Ram A. ; Aga, Mushtaq A. ; Jain, Shreyans K.

ChemInform, 2016-11, Vol.47 (49), p.no-no

Weinheim: WILEY‐VCH Verlag

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7
ChemInform Abstract: Direct Transformation of Ethylarenes into Primary Aromatic Amides with N‐Bromosuccinimide and I2—Aqueous NH3
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ChemInform Abstract: Direct Transformation of Ethylarenes into Primary Aromatic Amides with N‐Bromosuccinimide and I2—Aqueous NH3

Shimokawa, Shohei ; Kawagoe, Yuhsuke ; Moriyama, Katsuhiko ; Togo, Hideo

ChemInform, 2016-06, Vol.47 (27), p.no-no

Weinheim: WILEY‐VCH Verlag

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8
ChemInform Abstract: Synthesis of-Ketoamides by Copper-Catalyzed Reactions of Phenylacetic Acids with N,N-Dialkylformamides
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ChemInform Abstract: Synthesis of-Ketoamides by Copper-Catalyzed Reactions of Phenylacetic Acids with N,N-Dialkylformamides

Zhang, Lanping ; Pu, Junnan ; Ren, Jiayu ; Li, Zhengkai ; Xiang, Haifeng ; Zhou, Xiangge

ChemInform, 2015-12, Vol.46 (49), p.no-no

Weinheim: WILEY-VCH Verlag

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9
ChemInform Abstract: Indium(III) Chloride Promoted Highly Efficient Tandem Rearrangement—α‐Addition Strategy Towards the Synthesis of α‐Hydroxyamides
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ChemInform Abstract: Indium(III) Chloride Promoted Highly Efficient Tandem Rearrangement—α‐Addition Strategy Towards the Synthesis of α‐Hydroxyamides

Lingaswamy, Kadari ; Mohan, Dumpala ; Krishna, Palakodety Radha ; Prapurna, Y. Lakshmi

ChemInform, 2016-11, Vol.47 (47), p.no-no

Weinheim: WILEY‐VCH Verlag

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ChemInform Abstract: Efficient and Green Ritter Reaction for the Synthesis of N‐(t‐Butyl)‐ and N‐Benzylamides from t‐Butyl and Benzyl Acetates
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ChemInform Abstract: Efficient and Green Ritter Reaction for the Synthesis of N‐(t‐Butyl)‐ and N‐Benzylamides from t‐Butyl and Benzyl Acetates

Nasr‐Esfahani, Masoud ; Montazerozohori, Morteza ; Karami, Zeinab

ChemInform, 2016-11, Vol.47 (48), p.no-no

Weinheim: WILEY‐VCH Verlag

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