Literature DB >> 29115009

Divergent Total Syntheses of (-)-Daphnilongeranin B and (-)-Daphenylline.

Xiaoming Chen1, Hai-Jun Zhang1, Xinkan Yang2, Houqiang Lv2, Xiaoru Shao1, Cheng Tao2, Huifei Wang1, Bin Cheng2, Yun Li2, Jingjing Guo2, Jing Zhang1, Hongbin Zhai1,2,3.   

Abstract

(-)-Daphnilongeranin B and (-)-daphenylline are two hexacyclic Daphniphyllum alkaloids, each containing a complex cagelike backbone. Described herein are the first asymmetric total synthesis of (-)-daphnilongeranin B and a bioinspired synthesis of (-)-daphenylline with an unusual E ring embedded in a cagelike framework. The key features include an intermolecular [3+2] cycloaddition, a late-stage aldol cyclization to install the F ring of daphnilongeranin B, and a bioinspired cationic rearrangement leading to the tetrasubstituted benzene ring of daphenylline.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  [3+2] cycloaddition; alkaloids; asymmetric total synthesis; natural products; rearrangement

Year:  2017        PMID: 29115009     DOI: 10.1002/anie.201709762

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


  5 in total

1.  Calyciphylline B-Type Alkaloids: Total Syntheses of (-)-Daphlongamine H and (-)-Isodaphlongamine H.

Authors:  Cedric L Hugelshofer; Vignesh Palani; Richmond Sarpong
Journal:  J Am Chem Soc       Date:  2019-05-16       Impact factor: 15.419

2.  Phosphine-Catalyzed α-Umpolung-Aldol Reaction for the Synthesis of Benzo[ b]azapin-3-ones.

Authors:  Kui Zhang; Lingchao Cai; Sooji Hong; Ohyun Kwon
Journal:  Org Lett       Date:  2019-06-20       Impact factor: 6.005

3.  Tin-Free Access to the ABC Core of the Calyciphylline A Alkaloids and Unexpected Formation of a D-Ring-Contracted Tetracyclic Core.

Authors:  Alberto M Lopez; Ahmad A Ibrahim; Gregory J Rosenhauer; Hansamali S Sirinimal; Jennifer L Stockdill
Journal:  Org Lett       Date:  2018-04-03       Impact factor: 6.005

Review 4.  All-carbon [3 + 2] cycloaddition in natural product synthesis.

Authors:  Zhuo Wang; Junyang Liu
Journal:  Beilstein J Org Chem       Date:  2020-12-09       Impact factor: 2.883

5.  Synthetic studies toward longeracemine: a SmI2-mediated spirocyclization and rearrangement cascade to construct the 2-azabicyclo[2.2.1]heptane framework.

Authors:  Keita Komine; Kyle M Lambert; Quentin R Savage; Joshua B Cox; John L Wood
Journal:  Chem Sci       Date:  2020-07-30       Impact factor: 9.825

  5 in total

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