Diastereoselective Tandem 6-exo Carbolithiation Intramolecular Ring Opening in (−)-8-Aminomenthol-Derived Perhydrobenzoxazines. A New Synthesis of Enantiopure 4-Substituted Tetrahydro Isoquinolines and 2-Azabenzonorbornanes-Reference-Cited by-同舟云学术

Diastereoselective Tandem 6-exo Carbolithiation Intramolecular Ring Opening in (−)-8-Aminomenthol-Derived Perhydrobenzoxazines. A New Synthesis of Enantiopure 4-Substituted Tetrahydro Isoquinolines and 2-Azabenzonorbornanes

Published:2001-02-06 Issue:9 Volume:123 Page:1817-1821
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Pedrosa Rafael¹,Andrés Celia¹,Iglesias Jesús M.¹,Pérez-Encabo Alfonso¹

Affiliation:

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

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja002864q

Reference47 articles.

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3. Anionic cyclization of olefinic alkyllithiums: ring closure of terminally substituted 5-hexenyllithiums.

4. Lithium−Iodine Exchange Mediated Atom Transfer Cyclization: Catalytic Cycloisomerization of 6-Iodo-1-hexenes

5. Catalytic Cycloisomerization of Unsaturated Organoiodides

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