Photolysis of phenacyl esters in a two-phase system

Synthetic Communications

Volumn 32, Issue 16, 2002, Pages 2581-2590

  Ruzicka, Radovan ^a   Zabadal, Miroslav ^a   Klán, Petr ^a  

^a MASARYK UNIVERSITY   (Czech Republic)

Author keywords

Phenacyl; Photochemistry; Protecting group; Two phase system

Indexed keywords

2,5 DIMETHYLPHENACYL ESTER DERIVATIVE; CETRIMIDE; ESTER DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ARTICLE; MOLECULAR DYNAMICS; PHOTOCHEMISTRY; PHOTOLYSIS; REACTION ANALYSIS; SYNTHESIS;

EID: 0036329835     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120005943     Document Type: Article

References (26)

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2. New phototriggers 9: p-Hydroxyphenacyl as a C-terminal photoremovable protecting group for oligopeptides
3. New photoactivated protecting groups 6. p-Hydroxyphenacyl: A phototrigger for chemical and biochemical probes
4. New phototriggers: Extending the p-hydroxyphenacyl pi-pi* absorption range
5. p-Hydroxyphenacyl phototriggers the reactive excited state of phosphate photorelease
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11. Protecting groups that can be removed through photochemical electron transfer: Mechanistic and product studies on photosensitized release of carboxylates from phenacyl esters
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13. Direct photolysis of phenacyl protecting groups studied by laser flash photolysis: An excited state hydrogen atom abstraction pathway leads to formation of carboxylic acids and acetophenone
14. 2,5-Dimethylphenacyl as a new photoreleasable protecting group for carboxylic acids
15. 2,5-Dimethylphenacyl esters: A photoremovable protecting group for carboxylic acids
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21. Photorelease of HCl from o-methylphenacyl chloride proceeds through the Z-xylylenol