Related Experiment Video
Updated: Jun 13, 2026

Synthesis of Single-Crystalline Core-Shell Metal-Organic Frameworks
Published on: February 10, 2023
Straightforward assembly of the octahydroisoquinoline core of morphinan alkaloids
Julie Dunet1, Raphaël Lebeuf, Gopal Bose
1Université de Bordeaux, Institut des Sciences Moléculaires, UMR-CNRS 5255, 351, cours de la libération, 33405 Talence cedex 05, France.
Abstract:
The octahydroisoquinoline core of morphinan was assembled starting from readily available arylcyclohexadienes. Three different approaches were developed, including a metal- and an acid-mediated Mannich type process and an anionic-mediated cyclization. All provided the desired motif as a single diastereomer having a C9-C13-C14 trans-cis relative configuration.
Related Concept Videos
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous overlap of p...
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group with both...
Formation of Halohydrin from Alkenes
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism
Opioid Analgesics: Synthetic and Semisynthetic Opioids
Assembly of Complex Microtubule Structures

![Solid-phase Synthesis of [4.4] Spirocyclic Oximes](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F58508.jpg&w=3840&q=50)