Journal
ORGANIC LETTERS
Volume 17, Issue 14, Pages 3430-3433Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b01432
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- DST, New Delhi [SR/S1/OC-97/2012]
- CBMR, Lucknow
- CSIR, New Delhi
- UGC, New Delhi
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An efficient strategy for the synthesis of 3-(3-indolyl)-oxindole-3-methanol has been developed to achieve a Lewis acid catalyzed, highly regioselective ring opening of spiro-epoxyoxindoles with indoles. The method is used for the gram-scale formal total synthesis of (+/-)-gliocladin C.
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