Literature DB >> 23613314

Highly enantioselective inverse-electron-demand hetero-Diels-Alder reactions catalyzed by modularly designed organocatalysts.

Debarshi Sinha1, Sandun Perera, John Cong-Gui Zhao.   

Abstract

Year:  2013        PMID： 23613314     DOI： 10.1002/chem.201300168

Source DB:  PubMed          Journal:  Chemistry        ISSN： 0947-6539            Impact factor:   5.236


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  3 in total

1.  Diastereodivergent Synthesis of Hexahydro-6H-benzo[c]chromen-6-one Derivatives Catalyzed by Modularly Designed Organocatalysts.

Authors:  Satish Jakkampudi; Ramarao Parella; Hadi D Arman; John C-G Zhao
Journal:  Chemistry       Date:  2019-05-09       Impact factor: 5.236

2.  Stereoselective synthesis of chromane derivatives via a domino reaction catalyzed by modularly designed organocatalysts.

Authors:  Satish Jakkampudi; Ramarao Parella; John C-G Zhao
Journal:  Org Biomol Chem       Date:  2018-12-19       Impact factor: 3.876

Review 3.  Recent Advances in Inverse-Electron-Demand Hetero-Diels-Alder Reactions of 1-Oxa-1,3-Butadienes.

Authors:  Aleksandra Pałasz
Journal:  Top Curr Chem (Cham)       Date:  2016-04-20
  3 in total

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