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Increasing Rates and Scope of Reactions: Sluggish Amines in Microwave-Heated Aminocarbonylation Reactions under Air

Journal of organic chemistry, 2003-07, Vol.68 (14), p.5750-5753

2003

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Characterization of a human and murine mPGES-1 inhibitor and comparison to mPGES-1 genetic deletion in mouse models of inflammation

Prostaglandins & other lipid mediators, 2013-12, Vol.107, p.26-34

2013

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One-Pot, Two-Step, Microwave-Assisted Palladium-Catalyzed Conversion of Aryl Alcohols to Aryl Fluorides via Aryl Nonaflates

Journal of organic chemistry, 2013-04, Vol.78 (8), p.4184-4189

2013

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Microwave Promoted Transcarbamylation Reaction of Sulfonylcarbamates under Continuous-Flow Conditions

Organic process research & development, 2016-02, Vol.20 (2), p.440-445

2016

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Biological characterization of new inhibitors of microsomal PGE synthase‐1 in preclinical models of inflammation and vascular tone

British journal of pharmacology, 2019-12, Vol.176 (24), p.4625-4638

2019

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Identification of novel and potent inhibitors of SARS-CoV-2 main protease from DNA-encoded chemical libraries

Antimicrobial agents and chemotherapy, 2024, Vol.68 (10), p.e0090924

2024

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Synthesis of enantiopure angiotensin II type 2 receptor [AT2R] antagonist EMA401

Tetrahedron, 2015-09, Vol.71 (38), p.6881-6887

2015

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A convenient transesterification method for synthesis of AT2 receptor ligands with improved stability in human liver microsomes

Bioorganic & medicinal chemistry letters, 2018-02, Vol.28 (3), p.519-522

2018

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N-(Heteroaryl)thiophene sulfonamides as angiotensin AT2 receptor ligands

European journal of medicinal chemistry, 2024-02, Vol.265, p.116122-116122, Article 116122

2024

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Rapid and straightforward transesterification of sulfonyl carbamates

Tetrahedron letters, 2016-03, Vol.57 (13), p.1476-1478

2016

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N-(Methyloxycarbonyl)thiophene sulfonamides as high affinity AT2 receptor ligands

Bioorganic & medicinal chemistry, 2021-01, Vol.29, p.115859-115859, Article 115859

2021

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Hydroxylamine as an ammonia equivalent in microwave-enhanced aminocarbonylations

Tetrahedron, 2006-05, Vol.62 (19), p.4665-4670

2006

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Microwave Heated Flow Synthesis of Spiro-oxindole Dihydroquinazolinone Based IRAP Inhibitors

Organic process research & development, 2014-11, Vol.18 (11), p.1582-1588

2014

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A Series of Analogues to the AT2R Prototype Antagonist C38 Allow Fine Tuning of the Previously Reported Antagonist Binding Mode

ChemistryOpen (Weinheim), 2019-01, Vol.8 (1), p.114-125

2019

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HIV-1 Protease Inhibitors with a Transition-State Mimic Comprising a Tertiary Alcohol: Improved Antiviral Activity in Cells

Journal of medicinal chemistry, 2010-01, Vol.53 (2), p.607-615

2010

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A Series of Analogues to the AT 2 R Prototype Antagonist C38 Allow Fine Tuning of the Previously Reported Antagonist Binding Mode

ChemistryOpen (Weinheim), 2019-01, Vol.8 (1), p.114-125

2019

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Direct Microwave Synthesis of N,N′-Diacylhydrazines and Boc-Protected Hydrazides by in situ Carbonylations under Air

Synlett, 2004-11, Vol.2004 (13), p.2335-2338

2004

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Stereoselective Synthesis of 3-Aminoindan-1-ones and Subsequent Incorporation into HIV-1 Protease Inhibitors

Journal of organic chemistry, 2006-02, Vol.71 (3), p.1265-1268

2006

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A new structural theme in C 2-symmetric HIV-1 protease inhibitors: ortho-Substituted P1/P1′ side chains

Bioorganic & medicinal chemistry, 2006-08, Vol.14 (15), p.5303-5315

2006

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A new structural theme in C2-symmetric HIV-1 protease inhibitors : ortho-Substituted P1/P1' side chains

Bioorganic & medicinal chemistry, 2006-08, Vol.14 (15), p.5303-5315

2006

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A facilitated approach to evaluate the inhibitor mode and potency of compounds targeting microsomal prostaglandin e synthase-1

Assay and drug development technologies, 2011-10, Vol.9 (5), p.487-495

2011

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A new structural theme in C sub(2)-symmetric HIV-1 protease inhibitors: ortho-Substituted P1/P1' side chains

Bioorganic & medicinal chemistry, 2006-08, Vol.14 (15), p.5303-5315

2006

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Microwave-assisted synthesis of c2-symmetric hiv-1 protease inhibitors: development and applications of in situ carbonylations and other palladium(0)-catalyzed reactions

Wannberg, Johan

2005

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Microwave-Accelerated Synthesis of Protease Inhibitors

Microwave Methods in Organic Synthesis, 2006, p.167-198

2006

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ChemInform Abstract: Rapid and Straightforward Transesterification of Sulfonyl Carbamates

ChemInform, 2016-06, Vol.47 (29), p.no-no

2016

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Increasing Rates and Scope of Reactions: Sluggish Amines in Microwave-Heated Aminocarbonylation Reactions under Air

Characterization of a human and murine mPGES-1 inhibitor and comparison to mPGES-1 genetic deletion in mouse models of inflammation

One-Pot, Two-Step, Microwave-Assisted Palladium-Catalyzed Conversion of Aryl Alcohols to Aryl Fluorides via Aryl Nonaflates

Microwave Promoted Transcarbamylation Reaction of Sulfonylcarbamates under Continuous-Flow Conditions

Biological characterization of new inhibitors of microsomal PGE synthase‐1 in preclinical models of inflammation and vascular tone

Identification of novel and potent inhibitors of SARS-CoV-2 main protease from DNA-encoded chemical libraries

Synthesis of enantiopure angiotensin II type 2 receptor [AT2R] antagonist EMA401

A convenient transesterification method for synthesis of AT2 receptor ligands with improved stability in human liver microsomes

N-(Heteroaryl)thiophene sulfonamides as angiotensin AT2 receptor ligands

Rapid and straightforward transesterification of sulfonyl carbamates

N-(Methyloxycarbonyl)thiophene sulfonamides as high affinity AT2 receptor ligands

Hydroxylamine as an ammonia equivalent in microwave-enhanced aminocarbonylations

Microwave Heated Flow Synthesis of Spiro-oxindole Dihydroquinazolinone Based IRAP Inhibitors

A Series of Analogues to the AT2R Prototype Antagonist C38 Allow Fine Tuning of the Previously Reported Antagonist Binding Mode

HIV-1 Protease Inhibitors with a Transition-State Mimic Comprising a Tertiary Alcohol: Improved Antiviral Activity in Cells

A Series of Analogues to the AT 2 R Prototype Antagonist C38 Allow Fine Tuning of the Previously Reported Antagonist Binding Mode

Direct Microwave Synthesis of N,N′-Diacylhydrazines and Boc-Protected Hydrazides by in situ Carbonylations under Air

Stereoselective Synthesis of 3-Aminoindan-1-ones and Subsequent Incorporation into HIV-1 Protease Inhibitors

A new structural theme in C 2-symmetric HIV-1 protease inhibitors: ortho-Substituted P1/P1′ side chains

A new structural theme in C2-symmetric HIV-1 protease inhibitors : ortho-Substituted P1/P1' side chains

A facilitated approach to evaluate the inhibitor mode and potency of compounds targeting microsomal prostaglandin e synthase-1

A new structural theme in C sub(2)-symmetric HIV-1 protease inhibitors: ortho-Substituted P1/P1' side chains

Microwave-assisted synthesis of c2-symmetric hiv-1 protease inhibitors: development and applications of in situ carbonylations and other palladium(0)-catalyzed reactions

Microwave-Accelerated Synthesis of Protease Inhibitors

ChemInform Abstract: Rapid and Straightforward Transesterification of Sulfonyl Carbamates

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