Practical Isolation of the (1R,2R)-Enantiomer from a Racemic cis/trans Mixture of 2-Methyl-1-cyclohexanamine-Reference-Cited by-同舟云学术

Practical Isolation of the (1R,2R)-Enantiomer from a Racemic cis/trans Mixture of 2-Methyl-1-cyclohexanamine

Published:2017-10-17 Issue:11 Volume:21 Page:1822-1827
ISSN:1083-6160
Container-title:Organic Process Research & Development
language:en
Short-container-title:Org. Process Res. Dev.

Author:

Furegati Markus¹^ORCID,Nocito Sandro¹

Affiliation:

1. Synthesis & Technologies Group, Global Discovery Chemistry, Novartis Institutes for Biomedical Research, Klybeckstrasse 141, 4057 Basel, Switzerland

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.7b00263

Reference14 articles.

1. Über die Stereochemie der Hexahydro‐toluidine

2. The Resolution and Rotations oftrans-2-Aminocyclohexanecarboxylic Acids and Derivatives

3. Organoboranes for synthesis. 7. An improved general synthesis of primary amines from alkenes via hydroboration-organoborane chemistry

4. A Stereospecific Synthesis of Alicyclic and Bicyclic Amines via Hydroboration

5. Organoboranes. 46. New procedures for the homologation of boronic esters. A critical examination of the available procedures to achieve convenient homologation of boronic esters

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