Literature DB >> 26621771

Synthetic approaches towards alkaloids bearing α-tertiary amines.

Anastasia Hager1, Nina Vrielink, Dominik Hager, Julien Lefranc, Dirk Trauner.   

Abstract

Alkaloids account for some of the most beautiful and biologically active natural products. Although they are usually classified along biosynthetic criteria, they can also be categorized according to certain structural motifs. Amongst these, the α-tertiary amine (ATA), i.e. a tetrasubstituted carbon atom surrounded by three carbons and one nitrogen, is particularly interesting. A limited number of methods have been described to access this functional group and fewer still are commonly used in synthesis. Herein, we review some approaches to asymmetrically access ATAs and provide an overview of alkaloid total syntheses where those have been employed.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 26621771     DOI: 10.1039/c5np00096c

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  20 in total

1.  Total Synthesis of the Norhasubanan Alkaloid Stephadiamine.

Authors:  Nina Hartrampf; Nils Winter; Gabriele Pupo; Brian M Stoltz; Dirk Trauner
Journal:  J Am Chem Soc       Date:  2018-07-09       Impact factor: 15.419

2.  Second-Generation Palladium Catalyst System for Transannular C-H Functionalization of Azabicycloalkanes.

Authors:  Pablo J Cabrera; Melissa Lee; Melanie S Sanford
Journal:  J Am Chem Soc       Date:  2018-04-13       Impact factor: 15.419

3.  Enantioselective Markovnikov Addition of Carbamates to Allylic Alcohols for the Construction of α-Secondary and α-Tertiary Amines.

Authors:  Ana Bahamonde; Buthainah Al Rifaie; Victor Martín-Heras; Jamie R Allen; Matthew S Sigman
Journal:  J Am Chem Soc       Date:  2019-05-24       Impact factor: 15.419

4.  Multicomponent alkene azidoarylation by anion-mediated dual catalysis.

Authors:  Ala Bunescu; Yusra Abdelhamid; Matthew J Gaunt
Journal:  Nature       Date:  2021-09-13       Impact factor: 49.962

5.  Site-Selective α-C-H Functionalization of Trialkylamines via Reversible Hydrogen Atom Transfer Catalysis.

Authors:  Yangyang Shen; Ignacio Funez-Ardoiz; Franziska Schoenebeck; Tomislav Rovis
Journal:  J Am Chem Soc       Date:  2021-11-05       Impact factor: 15.419

6.  Enantioconvergent Amination of Racemic Tertiary C-H Bonds.

Authors:  Kai Lang; Chaoqun Li; Isaac Kim; X Peter Zhang
Journal:  J Am Chem Soc       Date:  2020-11-29       Impact factor: 15.419

7.  CuH-Catalyzed Regio- and Enantioselective Hydrocarboxylation of Allenes: Toward Carboxylic Acids with Acyclic Quaternary Centers.

Authors:  Sheng Feng; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2021-03-24       Impact factor: 15.419

8.  Dearomative Synthetic Entry into the Altemicidin Alkaloids.

Authors:  Claire S Harmange Magnani; Thomas J Maimone
Journal:  J Am Chem Soc       Date:  2021-05-21       Impact factor: 16.383

9.  1,3-Dipolar cycloaddition of isatin N,N'-cyclic azomethine imines with α,β-unsaturated aldehydes catalyzed by DBU in water.

Authors:  Zhan-Yong Wang; Ting Yang; Rongxiang Chen; Xueji Ma; Huan Liu; Kai-Kai Wang
Journal:  RSC Adv       Date:  2020-06-25       Impact factor: 4.036

10.  Stereocontrolled Total Synthesis of (-)-Stemaphylline.

Authors:  Ana Varela; Lennart K B Garve; Daniele Leonori; Varinder K Aggarwal
Journal:  Angew Chem Int Ed Engl       Date:  2017-01-18       Impact factor: 15.336

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.