Amanote Research
Register
Sign In
New Procedure to Mask the 2, 3-P Bond of the Indole Nucleus and Its Application to the Preparation of Potent Opioid Receptor Agonists With a Corynanthe Skeleton
doi 10.1021/ol062173k.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Highly Potent and Selective Phenylmorphan-Based Inverse Agonists of the Opioid D Receptor
New Small Molecule Agonists to the Thyrotropin Receptor
Thyroid
Medicine
Endocrinology
Metabolism
Diabetes
A New Method for Introducing Some Active Methylene or Methine Groups to the 3-Position of Pyrrolidine or Piperidine Skeleton, and Its Application to Preparation of a Key Intermediate for (±)-Eburnamonine Synthesis
Chemistry Letters
Chemistry
Irreversible Binding Ofcis--3-Methylfentanyl Isothiocyanate to the Opioid Receptor and Determination of Its Binding Domain
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Anti-Obesity Effects of Selective Agonists to the .BETA.3-Adrenergic Receptor in Dogs. I. The Presence of Canine .BETA.3-Adrenergic Receptor and in Vivo Lipomobilization by Its Agonists.
Journal of Veterinary Medical Science
Veterinary
Novel Alternative for the N-S Bond Formation and Its Application to the Synthesis of Benzisothiazol-3-Ones
The Identification of the 2-Phenylphthalazin-1(2h)-One Scaffold as a New Decorable Core Skeleton for the Design of Potent and Selective Human A3Adenosine Receptor Antagonists
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Aromatic Hydrocarbon Responsiveness-Receptor Agonists Generated From Indole-3-Carbinol in Vitro and in Vivo: Comparisons With 2,3,7,8-Tetrachlorodibenzo-P-Dioxin.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Novel Preparation of 3-Hydroxy-3h-Indole-3-Ethanamines and -3h-Indole-3-Acetamides Having Either a 4-Morpholinyl or 1-Pyrrolidinyl Group at the 2-Position.
ChemInform