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Correction: Stereoselective synthesis of (−)-desethyleburnamonine, (−)-vindeburnol and (−)-3-epitacamonine: observation of a substrate dependent diastereoselectivity reversal of an aldol reaction
Pravat
Mondal
and
Narshinha P.
Argade
*
Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India. E-mail: np.argade@ncl.res.in
First published on 24th October 2016
Abstract
Correction for ‘Stereoselective synthesis of (−)-desethyleburnamonine, (−)-vindeburnol and (−)-3-epitacamonine: observation of a substrate dependent diastereoselectivity reversal of an aldol reaction’ by Pravat Mondal et al., Org. Biomol. Chem., 2016, DOI: 10.1039/c6ob01438k.
The authors regret that two references to the literature procedure for the transformation of compound 3 to compound 4 were omitted in Scheme 1. The correct scheme and references are shown below.
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| Scheme 1 Stereoselective synthesis of (±)-keto-lactam and (+)-keto-amine precursors for ester aldol reactions. | ||
14 P.-Q. Huang, L.-X. Liu, B.-G. Wei, Y.-P. Ruan, Org. Lett., 2003, 5, 1927.
15 Y.-P. Ruan, B.-G. Wei, X.-Q. Xu, G. Liu, D.-S. Yu, L.-X. Liu, P.-Q. Huang, Chirality, 2005, 17, 595.
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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