An improved protocol for azole synthesis with PEG-supported Burgess reagent

Tetrahedron Letters

Volumn 37, Issue 27, 1996, Pages 4659-4662

  Wipf, Peter ^a   Venkatraman, Srikanth ^a  

^a UNIVERSITY OF PITTSBURGH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

OXAZOLINE DERIVATIVE; THIAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG SYNTHESIS; REACTION ANALYSIS; STEREOCHEMISTRY; TECHNIQUE;

EID: 0030199693     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)00918-5     Document Type: Article

References (22)

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3. (c) van Koten, G. Pure Appl. Chem. 1994, 66, 1455.
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5. 2. Atkins, G. M.; Burgess, E. M. J. Am. Chem. Soc. 1968, 90, 4744.
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11. 4. See, for example: (a) Wipf, P.; Miller, C. P. J. Am. Chem. Soc. 1992, 114, 10975.
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21. 2 (EtOAc/Hexanes 1:1) to yield 85 mg (90%) of the desired oxazoline as a colorless oil. For the spectroscopic characterization of this oxazoline, see ref. 4a.
22. 6. These experiments were performed by Mr. Greg Hayes in the context of synthetic studies toward phenoxan in our laboratories.