A New Efficient Route to Tolterodine-Reference-Cited by-同舟云学术

A New Efficient Route to Tolterodine

Published:2002-05-18 Issue:4 Volume:6 Page:379-383
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Botteghi Carlo¹,Corrias Tatiana¹,Marchetti Mauro¹,Paganelli Stefano¹,Piccolo Oreste¹

Affiliation:

1. Dipartimento di Chimica - Università Ca' Foscari di Venezia, Calle Larga S. Marta 2137, I-30123 Venezia, Italy, Istituto di Chimica Biomolecolare - CNR, traversa La Crucca 3, Loc. Baldinca - Li Punti, I-07040 Sassari, Italy, and Studio di Consulenza Scientifica, via Bornò 5, Sirtori (LC), Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op020014k

Reference28 articles.

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3. Based onIndex of Drug Chemicals in the Ten More IndustrializedCountries; IMS Health: London, U.K., 2000.

4. Jonsson, N. A.; Sparf, B. A.; Mikiver, L.; Moses, P.; Nilvebrant, L.; Glas, G. (Pharmacia & Upjohn Co.). EP 0325571,1989.

5. Asymmetric Total Synthesis of (+)-Tolterodine, a New Muscarinic Receptor Antagonist, via Copper-Assisted Asymmetric Conjugate Addition of Aryl Grignard Reagents to 3-Phenyl-prop-2-enoyl-oxazolidinones

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