Journal of the Chemical Society. Chemical communications p. 762 - 764 (1993)
Update date:2022-08-17
Topics:
Lopez, J. Cristobal
Gomez, Ana M.
Reid-Fraser, Bert
Stereoselective addition of carbon branches at C(1) and C(2) of L-rhamnal is achieved via silicon-mediated radical procedures, and the product is readily processed to give a hex-2-enopyranosid-4-ulose whose intramolecular Diels-Alder reaction has been examined.
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