Efficient Synthesis of 8-Oxa-3-aza-bicyclo[3.2.1]octane Hydrochloride-Reference-Cited by-同舟云学术

Efficient Synthesis of 8-Oxa-3-aza-bicyclo[3.2.1]octane Hydrochloride

Published:2010-02-16 Issue:2 Volume:14 Page:459-465
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Connolly Terrence J.¹,Considine John L.¹,Ding Zhixian¹,Forsatz Brian¹,Jennings Mellard N.¹,MacEwan Michael F.¹,McCoy Kevin M.¹,Place David W.¹,Sharma Archana¹,Sutherland Karen¹

Affiliation:

1. Chemical Development, Wyeth Research, 401 North Middletown Road, Pearl River, New York 10965, U.S.A.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/op9002642

Reference21 articles.

1. Early Process Development: The Wyeth Approach

2. Aminoalcohols Containing the 8-Oxa-3-azabicyclo [3.2.1]octane Ring System and Their Benzoates

3. 1. The conversion of sucrose into furan compounds. Part II. Some 2 : 5-disubstituted tetrahydrofurans and their products of ring scission

4. Screening was performed using an Endeavor Catalyst Screening System from Biotage/Argonaut.

5. 13C NMR supported the 95/5 ratio of isomers determined by GC. See theExperimental Sectionfor line listings of both the major and minor isomer.

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