Solution and Solid-State Conformational and Structural Analysis of the N-Methyl Derivatives of (±)-threo-Methylphenidate, (±)-erythro-Methylphenidate, and (±)-threo-p-Methyl-methylphenidate Hydrochloride Salts-Reference-Cited by-同舟云学术

Solution and Solid-State Conformational and Structural Analysis of the N-Methyl Derivatives of (±)-threo-Methylphenidate, (±)-erythro-Methylphenidate, and (±)-threo-p-Methyl-methylphenidate Hydrochloride Salts

Published:1998-02-26 Issue:6 Volume:63 Page:1785-1794
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Glaser Robert,Adin Itay,Shiftan Dror,Shi Qing,Deutsch Howard M.,George Clifford¹,Wu Kuo-Ming,Froimowitz Mark

Affiliation:

1. Laboratory for the Structure of Matter, Naval Research Laboratory, Washington, D.C. 20375-0001

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971063b

Reference37 articles.

1. The Merck Index, 11th ed.; Budavari, S., Ed.; Merck: Rahway, 1989; p 960 and references therein.

2. Investigations into the correlations between monoamine oxidase inhibition and other effects due to methylphenydate and its stereoisomers

3. Absolute configurations of the pheniramines, methyl phenidates, and pipradrols

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