Synthesis of Enantiopure Highly Substituted trans-8a-Hydroxydecahydroisoquinolines by Sequential Diastereoselective IMDA Reaction and Oxanorbornene Nucleophilic Ring Opening-Reference-Cited by-同舟云学术

Synthesis of Enantiopure Highly Substituted trans-8a-Hydroxydecahydroisoquinolines by Sequential Diastereoselective IMDA Reaction and Oxanorbornene Nucleophilic Ring Opening

Published:1998-10-28 Issue:23 Volume:63 Page:8570-8573
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Andrés Celia¹,Nieto Javier¹,Pedrosa Rafael¹,Vicente Martina¹

Affiliation:

1. Departamento de Química Orgánica, Facultad de Ciencias, Universidad de Valladolid, Dr. Mergelina s/n, 47011-Valladolid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo981075c

Reference24 articles.

1. Pyridines and their Benzo Derivatives: (v) Synthesis

2. Overman, L. E.; Ricca, D. J. InComprehensive Organic Synthesis; Heathcock, C. H., Ed.; Pergamon: Oxford, U.K., 1991; Vol. 2, p 1007.

3. 2,3,4,4a,5,6,7,7a-Octahydro-1H-benzofuro[3,2-e]isoquinoline: a new morphine fragment

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