Literature DB >> 18830991

Organocatalytic approach to benzofused nitrogen-containing heterocycles: enantioselective total synthesis of (+)-angustureine.

Santos Fustero1, Javier Moscardó, Diego Jiménez, María Dolores Pérez-Carrión, María Sánchez-Roselló, Carlos Del Pozo.   

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Year:  2008        PMID: 18830991     DOI: 10.1002/chem.200801480

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


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  6 in total

1.  Enantioselective approach to quinolizidines: total synthesis of cermizine D and formal syntheses of senepodine G and cermizine C.

Authors:  Nagarathanam Veerasamy; Erik C Carlson; Nathan D Collett; Mrinmoy Saha; Rich G Carter
Journal:  J Org Chem       Date:  2013-04-29       Impact factor: 4.354

2.  Bifunctional cinchona alkaloid-squaramide-catalyzed highly enantioselective aza-Michael addition of indolines to α,β-unsaturated ketones.

Authors:  Arun K Ghosh; Bing Zhou
Journal:  Tetrahedron Lett       Date:  2013-07-03       Impact factor: 2.415

3.  Synthesis of Cyclic α-Aminophosphonates through Copper Catalyzed Enamine Activation.

Authors:  Junbin Han; Robert S Paton; Bo Xu; Gerald B Hammond
Journal:  Synthesis (Stuttg)       Date:  2013-02-01       Impact factor: 3.157

4.  Synthesis of Pyrrolidines and Pyrroles via Tandem Amination/Cyanation/Alkylation and Amination/Oxidation Sequences.

Authors:  Junbin Han; Zhichao Lu; Gerald B Hammond; Bo Xu
Journal:  European J Org Chem       Date:  2014-09-01

5.  An intramolecular C-N cross-coupling of β-enaminones: a simple and efficient way to precursors of some alkaloids of Galipea officinalis.

Authors:  Hana Doušová; Radim Horák; Zdeňka Růžičková; Petr Šimůnek
Journal:  Beilstein J Org Chem       Date:  2015-05-27       Impact factor: 2.883

Review 6.  Advances in the Asymmetric Total Synthesis of Natural Products Using Chiral Secondary Amine Catalyzed Reactions of α,β-Unsaturated Aldehydes.

Authors:  Zhonglei Wang
Journal:  Molecules       Date:  2019-09-19       Impact factor: 4.411

  6 in total

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