Preparation of 2,3-dihydro-1H-spiro[isoquinoline-4,4′-piperidine] via an N-sulfonyl Pictet–Spengler reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Design and biological activities of L-163,191 (MK-0677): a potent, orally active growth hormone secretagogue.
2. Peptidomimetic Growth Hormone Secretagogues. Design Considerations and Therapeutic Potential
3. The Synthesis of Spiro[tetrahydroisoquinoline-piperidines] and related compounds
4. Synthesis of 2,3,4,5-tetrahydro-7,8-dimethoxy-1H-2-benzazepines
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1. Design and synthesis of bridged piperidine and piperazine isosteres;Bioorganic & Medicinal Chemistry Letters;2018-08
2. Spiropiperidines;Privileged Structures in Drug Discovery;2018-03-09
3. Efficient and Practical One-Pot Conversions of N-Tosyltetrahydroisoquinolines into Isoquinolines and of N-Tosyltetrahydro-β-carbolines into β-Carbolines through Tandem β-Elimination and Aromatization;European Journal of Organic Chemistry;2010-11-03
4. Pictet-Spengler Reaction;Comprehensive Organic Name Reactions and Reagents;2010-09-15
5. Preparation of 3,4-fused-spiro[furan-5(5H),4′-piperidin]-2-one;Tetrahedron Letters;2009-09
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