Rhodium-mediated insertion of CF3-substituted carbenoid into O-H: An efficient method for the synthesis of α-trifluoromethylated alkoxy- and aryloxyacetic acid derivatives

Tetrahedron

Volumn 51, Issue 17, 1995, Pages 5011-5018

  Shi, Guo qiang ^a   Zhi yao Cao, ^a   Wei ling Cai, ^a  

^a SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

3,3,3 TRIFLUOROPROPIONIC ACID DERIVATIVE; ACETIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; PRIORITY JOURNAL; REACTION ANALYSIS;

EID: 0028904369     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4020(95)98698-H     Document Type: Article

References (34)

1. New chiral dopants for ferroelectric liquid crystals
2. Optically Active Ketones with Intramolecular Hydrogen Bond
3. Induced smectic C* phases
4. Recent Advances in Trifluoromethylation.
5. New ferroelectric liquid crystals with a trifluoromethyl group
6. Transition-metal catalyzed decomposition of aliphatic diazo compounds — New results and applications in organic synthesis
7. A facile synthesis of α-trifluorodiazo compounds
8. Ethyl 3-trifluoro-2-diazo-propionate as a potentially useful CF3-containing building block: preparation and [Rh(OAc)2]2-catalysed reaction with nitriles
9. Eine neue Methode zur Darstellung α,β-ungesättiger Ketone. Zerfall der Diazoketone RCOCN2CH2R′
10. Diastereoselectivity in the OH insertion reactions of rhodium carbenoids derived from phenyldiazoacetates of homochiral alcohols