Literature DB >> 11707144

Highly regioselective and diastereoselective directed hydroformylation of allylic ethers: a new approach to propionate aldol synthesis.

I J Krauss1, C C Wang, J L Leighton.   

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Year:  2001        PMID: 11707144     DOI: 10.1021/ja016978t

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


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  6 in total

1.  Regioselective Reductive Cross-Coupling Reactions of Unsymmetrical Alkynes.

Authors:  Holly A Reichard; Martin McLaughlin; Ming Z Chen; Glenn C Micalizio
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2.  Synthesis of quaternary carbon centers via hydroformylation.

Authors:  X Sun; K Frimpong; K L Tan
Journal:  J Am Chem Soc       Date:  2010-09-01       Impact factor: 15.419

3.  Regioselective hydroformylation of allylic alcohols.

Authors:  Thomas E Lightburn; Omar A De Paolis; Ka H Cheng; Kian L Tan
Journal:  Org Lett       Date:  2011-04-19       Impact factor: 6.005

4.  Metallacycle-Mediated Cross-Coupling with Substituted and Electronically Unactivated Alkenes.

Authors:  Holly A Reichard; Glenn C Micalizio
Journal:  Chem Sci       Date:  2011       Impact factor: 9.825

5.  Distal-selective hydroformylation using scaffolding catalysis.

Authors:  Candice L Joe; Thomas P Blaisdell; Allison F Geoghan; Kian L Tan
Journal:  J Am Chem Soc       Date:  2014-06-06       Impact factor: 15.419

6.  Nickel(0)-catalyzed linear-selective hydroarylation of unactivated alkenes and styrenes with aryl boronic acids.

Authors:  Honggui Lv; Li-Jun Xiao; Dongbing Zhao; Qi-Lin Zhou
Journal:  Chem Sci       Date:  2018-07-18       Impact factor: 9.825

  6 in total

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