Literature DB >> 17471484

Enantioselective synthesis of protected amines by the catalytic asymmetric addition of hydrazoic acid to ketenes.

Xing Dai1, Takashi Nakai, Jan A C Romero, Gregory C Fu.   

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Year:  2007        PMID: 17471484     DOI: 10.1002/anie.200700697

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


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  7 in total

Review 1.  Enantioselective protonation.

Authors:  Justin T Mohr; Allen Y Hong; Brian M Stoltz
Journal:  Nat Chem       Date:  2009-08       Impact factor: 24.427

2.  Catalytic, asymmetric reactions of ketenes and ketene enolates.

Authors:  Daniel H Paull; Anthony Weatherwax; Thomas Lectka
Journal:  Tetrahedron       Date:  2009-08-22       Impact factor: 2.457

3.  Enantioselective nucleophilic catalysis: the synthesis of aza-beta-lactams through [2+2] cycloadditions of ketenes with azo compounds.

Authors:  Jacob M Berlin; Gregory C Fu
Journal:  Angew Chem Int Ed Engl       Date:  2008       Impact factor: 15.336

4.  Nucleophilic carbene catalyzed synthesis of 1,2 amino alcohols via azidation of epoxy aldehydes.

Authors:  Harit U Vora; Johannah R Moncecchi; Oleg Epstein; Tomislav Rovis
Journal:  J Org Chem       Date:  2008-12-19       Impact factor: 4.354

5.  Enantioselective nucleophile-catalyzed synthesis of tertiary alkyl fluorides via the α-fluorination of ketenes: synthetic and mechanistic studies.

Authors:  Sarah Yunmi Lee; Stefan Neufeind; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2014-06-12       Impact factor: 15.419

6.  Pd(OAc)2-catalyzed asymmetric hydrogenation of sterically hindered N-tosylimines.

Authors:  Jianzhong Chen; Zhenfeng Zhang; Bowen Li; Feilong Li; Yulin Wang; Min Zhao; Ilya D Gridnev; Tsuneo Imamoto; Wanbin Zhang
Journal:  Nat Commun       Date:  2018-11-27       Impact factor: 14.919

7.  Copper-Catalyzed Azide-Alkyne Cycloaddition of Hydrazoic Acid Formed In Situ from Sodium Azide Affords 4-Monosubstituted-1,2,3-Triazoles.

Authors:  Dominik Jankovič; Miha Virant; Martin Gazvoda
Journal:  J Org Chem       Date:  2022-02-11       Impact factor: 4.354

  7 in total

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