First, Second, and Third Generation Scalable Syntheses of Two Potent H3 Antagonists

Author:

Pippel Daniel J.1,Mills John E.1,Pandit Chennagiri R.1,Young Lana K.1,Zhong Hua M.1,Villani Frank J.1,Mani Neelakandha S.1

Affiliation:

1. Johnson & Johnson Pharmaceutical Research and Development, L.L.C., 3210 Merryfield Row, San Diego, California 92121, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Revealing the Hidden Complexity and Reactivity of Palladacyclic Precatalysts: The P(o-tolyl)3 Ligand Enables a Cocktail of Active Species Utilizing the Pd(II)/Pd(IV) and Pd(0)/Pd(II) Pathways for Efficient Catalysis;ACS Catalysis;2024-08-09

2. 1,4‐Diazepane Ring‐Based Systems;More Synthetic Approaches to Nonaromatic Nitrogen Heterocycles;2022-04-15

3. Histamine H3 receptor antagonists/inverse agonists: Where do they go?;Pharmacology & Therapeutics;2019-08

4. Pharmaceutical Salts;Handbook for Chemical Process Research and Development;2016-10-17

5. Reaction Workup;Handbook for Chemical Process Research and Development;2016-10-17

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