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Enantioselective Organocatalytic Reductive Amination

Journal of the American Chemical Society, 2006-01, Vol.128 (1), p.84-86

2006

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The acid promoted Petasis reaction of organotrifluoroborates with imines and enamines

Chemical communications (Cambridge, England), 2017-10, Vol.53 (81), p.11185-11188

Carrera, Diane E

2017

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Magnesium Ethoxide Promoted Conversion of Nitriles to Amidines and Its Application in 5,6-Dihydroimidazobenzoxazepine Synthesis

Organic letters, 2018-05, Vol.20 (9), p.2624-2627

2018

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Highly Diastereoselective α‑Arylation of Cyclic Nitriles

Organic letters, 2017-07, Vol.19 (13), p.3446-3449

2017

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An Efficient Second-Generation Manufacturing Process for the pan-RAF Inhibitor Belvarafenib

Organic process research & development, 2021-10, Vol.25 (10), p.2338-2350

2021

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Stereoselective Synthesis of the IDO Inhibitor Navoximod

Journal of organic chemistry, 2022-04, Vol.87 (7), p.4955-4960

2022

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Development of a Practical and Greener Process for the Dual Leucine Zipper Kinase Inhibitor GDC-0134 Comprising Two SNAr Reactions, Oxidation and Suzuki Coupling

Organic process research & development, 2022-02, Vol.26 (2), p.313-322

2022

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Manufacture of the PI3K β‑Sparing Inhibitor Taselisib. Part 2: Development of a Highly Efficient and Regioselective Late-Stage Process

Organic process research & development, 2019-05, Vol.23 (5), p.783-793

2019

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Process Development of the Synthesis and Purification of a Reactive Immuno-PET Conjugate Intermediate

Organic process research & development, 2016-02, Vol.20 (2), p.312-318

2016

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Development of a general, enantioselective organocatalytic Mukaiyama–Michael reaction with α,β-unsaturated aldehydes

Tetrahedron, 2009-08, Vol.65 (33), p.6746-6753

2009

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Development of a Scalable Strategy for the Synthesis of PI3Kδ Inhibitors: Selective and Efficient Functionalization of Purine Derivatives

Organic process research & development, 2013-01, Vol.17 (1), p.138-144

2013

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The acid promoted Petasis reaction of organotrifluoroborates with imines and enaminesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7cc04397j

Carrera, Diane E

2017-10

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Fit-for-purpose synthesis of dual leucine zipper kinase (DLK) inhibitor GNE-834

Tetrahedron letters, 2020-10, Vol.61 (43), p.152430, Article 152430

2020

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Development of a Practical and Greener Process for the Dual Leucine Zipper Kinase Inhibitor GDC-0134 Comprising Two S N Ar Reactions, Oxidation and Suzuki Coupling

Organic process research & development, 2022-02, Vol.26 (2), p.313-322

2022

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Development of a general, enantioselective organocatalytic Mukaiyama-Michael reaction with α,β-unsaturated aldehydes: 2008 Tetrahedron Prize for Creativity in Organic Chemistry. The Art of Synthesis: Methods, Strategies and Applications

Tetrahedron, 2009, Vol.65 (33)

2009

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ChemInform Abstract: Development of a General Enantioselective Organocatalytic Mukaiyama-Michael Reaction with α,β-Unsaturated Aldehydes

ChemInform, 2009-12, Vol.40 (51), p.no-no

2009

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Enantioselective Organocatalytic Reductive Amination

ChemInform, 2006-05, Vol.37 (21), p.no-no

2006

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UV-Stressed Daphnia pulex Increase Fitness through Uptake of Vitamin D3

PloS one, 2015-07, Vol.10 (7), p.e0131847-e0131847

2015

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1147-D Preclinical characterization of a novel claudin 18.2 targeting-ISAC with robust potency and acceptable safety profile

Journal for immunotherapy of cancer, 2023-11, Vol.11 (Suppl 2), p.A1838-A1838

2023

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UV-Stressed Daphnia pulex Increase Fitness through Uptake of Vitamin D3: e0131847

PloS one, 2015-07, Vol.10 (7)

2015

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Enantioselective Organocatalytic Reductive Amination

The acid promoted Petasis reaction of organotrifluoroborates with imines and enamines

Magnesium Ethoxide Promoted Conversion of Nitriles to Amidines and Its Application in 5,6-Dihydroimidazobenzoxazepine Synthesis

Highly Diastereoselective α‑Arylation of Cyclic Nitriles

An Efficient Second-Generation Manufacturing Process for the pan-RAF Inhibitor Belvarafenib

Stereoselective Synthesis of the IDO Inhibitor Navoximod

Development of a Practical and Greener Process for the Dual Leucine Zipper Kinase Inhibitor GDC-0134 Comprising Two SNAr Reactions, Oxidation and Suzuki Coupling

Manufacture of the PI3K β‑Sparing Inhibitor Taselisib. Part 2: Development of a Highly Efficient and Regioselective Late-Stage Process

Process Development of the Synthesis and Purification of a Reactive Immuno-PET Conjugate Intermediate

Development of a general, enantioselective organocatalytic Mukaiyama–Michael reaction with α,β-unsaturated aldehydes

Development of a Scalable Strategy for the Synthesis of PI3Kδ Inhibitors: Selective and Efficient Functionalization of Purine Derivatives

The acid promoted Petasis reaction of organotrifluoroborates with imines and enaminesElectronic supplementary information (ESI) available. See DOI: 10.1039/c7cc04397j

Fit-for-purpose synthesis of dual leucine zipper kinase (DLK) inhibitor GNE-834

Development of a Practical and Greener Process for the Dual Leucine Zipper Kinase Inhibitor GDC-0134 Comprising Two S N Ar Reactions, Oxidation and Suzuki Coupling

Development of a general, enantioselective organocatalytic Mukaiyama-Michael reaction with α,β-unsaturated aldehydes: 2008 Tetrahedron Prize for Creativity in Organic Chemistry. The Art of Synthesis: Methods, Strategies and Applications

ChemInform Abstract: Development of a General Enantioselective Organocatalytic Mukaiyama-Michael Reaction with α,β-Unsaturated Aldehydes

Enantioselective Organocatalytic Reductive Amination

ASPCAP: THE APOGEE STELLAR PARAMETER AND CHEMICAL ABUNDANCES PIPELINE

UV-Stressed Daphnia pulex Increase Fitness through Uptake of Vitamin D3

1147-D Preclinical characterization of a novel claudin 18.2 targeting-ISAC with robust potency and acceptable safety profile

UV-Stressed Daphnia pulex Increase Fitness through Uptake of Vitamin D3: e0131847

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