A new resolution procedure for the preparation of both (R)-(+)- and (S)-(-)-4-tert-butoxycyclopent-2-enone from racemic 4-tert-butoxycyclopent-2-enone and conversion of (R)-(+)-4-tert-butoxycyclopent-2-enone into (R)-(+)-4-acetoxycyclopent-2-enone. A new method for the determination of the enantiomeric purities of the resolved enones
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00015a035
Cited by 26 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Highly Reactive and Tracelessly Cleavable Cysteine‐Specific Modification of Proteins via 4‐Substituted Cyclopentenone;Angewandte Chemie International Edition;2018-09-03
2. Highly Reactive and Tracelessly Cleavable Cysteine-Specific Modification of Proteins via 4-Substituted Cyclopentenone;Angewandte Chemie;2018-08-03
3. Synthesis of Chiral Cyclopentenones;Chemical Reviews;2016-04-21
4. ChemInform Abstract: A New Resolution Procedure for the Preparation of Both (R)-(+)- and (S) -(-)-4-tert-Butoxycyclopent-2-enone from Racemic 4-tert- Butoxycyclopent-2-enone and Conversion of (R)-(+)-4-tert- Butoxycyclopent-2-enone into (R)-(+)-4-Acetoxyc;ChemInform;2010-08-22
5. The thio-adduct facilitated, enzymatic kinetic resolution of 4-hydroxycyclopentenone and 4-hydroxycyclohexenone;Org. Biomol. Chem.;2010
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