Application of Biocatalytic Reductive Amination for the Synthesis of a Key Intermediate to a CDK 2/4/6 Inhibitor
Author:
Affiliation:
1. Chemical and Analytical Research and Development, Pfizer Worldwide Research and Development, Groton Laboratories, Groton, Connecticut 06340, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.1c00255
Reference25 articles.
1. Early Adaptation and Acquired Resistance to CDK4/6 Inhibition in Estrogen Receptor–Positive Breast Cancer
2. Discovery of PF-06873600, a CDK2/4/6 Inhibitor for the Treatment of Cancer
3. cBehenna, D. C.; Chen, P.; Freeman-Cook, K. D.; Hoffman, R. L.; Jalaie, M.; Nagata, A.; Nair, S. K.; Ninkovic, S.; Ornelas, M. A.; Palmer, C. L.; Rui, E. Y. CDK 2/4/6 inhibitors. U.S. Patent Appl. 10,233,188, WO Appl. 20180331815, 2018.
4. A radical chlorodifluoromethylation protocol for late-stage difluoromethylation and its application to an oncology candidate
5. Developing a Multistep Continuous Manufacturing Process for (1R,2R)-2-Amino-1-methylcyclopentan-1-ol
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