Journal
ORGANIC LETTERS
Volume 13, Issue 4, Pages 692-695Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol102923h
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- European Union (EU) within the EST network BIOMEDCHEM [MEST-CT-2005-020580]
- Region Ile-de-France
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The insertion reaction of diazocarbonyls to acids could be performed smoothly in fluorinated alcohols in the absence of metal catalyst. This new procedure allowed the chemoselective preparation of various functionalized compounds such as acyloxyesters, depsipeptides, and sulfonate, phosphonate, or boronate derivatives.
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