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Iridium(I)-catalyzed stereospecific decarboxylative allylic amidation of chiral branched benzyl allyl imidodicarboxylates.
Org Lett. 2007 Nov 08; 9(23):4801-4.OL

Abstract

Ir(I)-catalyzed decarboxylative allylic amidation of chiral branched benzyl allyl imidodicarboxylates has been shown to proceed with complete retention of enantiomeric purity and configuration. The transformation is stereospecific and appears to be quite general, accommodating a wide range of R groups.

Authors+Show Affiliations

Department of Chemistry, The University of Texas at San Antonio, One UTSA Circle, San Antonio, TX 78249, USA.No affiliation info available

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

17935343

Citation

Singh, Om V., and Hyunsoo Han. "Iridium(I)-catalyzed Stereospecific Decarboxylative Allylic Amidation of Chiral Branched Benzyl Allyl Imidodicarboxylates." Organic Letters, vol. 9, no. 23, 2007, pp. 4801-4.
Singh OV, Han H. Iridium(I)-catalyzed stereospecific decarboxylative allylic amidation of chiral branched benzyl allyl imidodicarboxylates. Org Lett. 2007;9(23):4801-4.
Singh, O. V., & Han, H. (2007). Iridium(I)-catalyzed stereospecific decarboxylative allylic amidation of chiral branched benzyl allyl imidodicarboxylates. Organic Letters, 9(23), 4801-4.
Singh OV, Han H. Iridium(I)-catalyzed Stereospecific Decarboxylative Allylic Amidation of Chiral Branched Benzyl Allyl Imidodicarboxylates. Org Lett. 2007 Nov 8;9(23):4801-4. PubMed PMID: 17935343.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Iridium(I)-catalyzed stereospecific decarboxylative allylic amidation of chiral branched benzyl allyl imidodicarboxylates. AU - Singh,Om V, AU - Han,Hyunsoo, Y1 - 2007/10/13/ PY - 2007/10/16/pubmed PY - 2007/12/12/medline PY - 2007/10/16/entrez SP - 4801 EP - 4 JF - Organic letters JO - Org Lett VL - 9 IS - 23 N2 - Ir(I)-catalyzed decarboxylative allylic amidation of chiral branched benzyl allyl imidodicarboxylates has been shown to proceed with complete retention of enantiomeric purity and configuration. The transformation is stereospecific and appears to be quite general, accommodating a wide range of R groups. SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/17935343/Iridium_I__catalyzed_stereospecific_decarboxylative_allylic_amidation_of_chiral_branched_benzyl_allyl_imidodicarboxylates_ L2 - https://doi.org/10.1021/ol702115h DB - PRIME DP - Unbound Medicine ER -