Tandem crystallization strategies for resolution of 3,3,3‐trifluorolactic acid [CF 3 CH(OH)COOH] by chiral benzylamines-Reference-Cited by-同舟云学术

Tandem crystallization strategies for resolution of 3,3,3‐trifluorolactic acid [CF 3 CH(OH)COOH] by chiral benzylamines

Published:2019-09-30 Issue:11 Volume:31 Page:979-991
ISSN:0899-0042
Container-title:Chirality
language:en
Short-container-title:Chirality

Author:

Wong Lawrence W.‐Y.¹^ORCID,Vashchenko Elena V.¹²^ORCID,Zhao Ying¹,Sung Herman H.‐Y.¹^ORCID,Vashchenko Valerii V.¹²^ORCID,Mikhailenko Vadim²,Krivoshey Alexander I.²,Williams Ian D.¹^ORCID

Affiliation:

1. Department of ChemistryHong Kong University of Science and Technology Kowloon Hong Kong, China

2. Institute for Single CrystalsNational Academy of Sciences Kharkov Ukraine

Funder

National Academy of Sciences of Ukraine

Science and Technology Center in Ukraine

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chir.23127

Reference33 articles.

1. Synthesis and reactions of 2-Alkoxy-1,1,3,3,3-pentafluoropropenes as a synthon for trifluoromethylated compounds.

2. Isomorphic supramolecular structures via one-dimensional hydrogen bonding motifs in crystals of chiral difluorolactates, trichlorolactates and trifluorolactates

3. Chiral Recognition by Multicenter Single Proton Hydrogen Bonding of Trifluorolactates

4. Application of (S)-trifluorolactic acid for chiral derivatizing agent

5. Chiral Synthesis via Organoboranes. 40. Selective Reductions. 55. A Simple One-Pot Synthesis of the Enantiomers of Trifluoromethyloxirane. A General Synthesis in High Optical Purities of .alpha.-Trifluoromethyl Secondary Alcohols via the Ring-Cleavage Reactions of the Epoxide

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