Rapid Access to the Tricyclic Core of Calyciphylline A -Type Alkaloids Through Allyl Cyanate-to-Isocyanate Rearrangement-Reference-Cited by-同舟云学术

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Rapid Access to the Tricyclic Core of Calyciphylline A -Type Alkaloids Through Allyl Cyanate-to-Isocyanate Rearrangement

Published:2019-11-28 Issue:46 Volume:2019 Page:7590-7595
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Baidilov Daler¹^ORCID,Miskey Scott¹,Hudlicky Tomas¹^ORCID

Affiliation:

1. Department of Chemistry and Centre for Biotechnology; Brock University; 1812 Sir Isaac Brock Way L2S 3A1 St. Catharines ON Canada

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201901549/fullpdf

Reference26 articles.

1. Calyciphyllines A and B, Two Novel Hexacyclic Alkaloids from Daphniphyllum calycinum

2. Recent Progress in the Chemistry of Daphniphyllum Alkaloids

3. Total synthesis of the Daphniphyllum alkaloid daphenylline

4. Total Synthesis of (−)‐Daphenylline

5. Total Synthesis of (−)‐Daphenylline

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Total Synthesis of Daphniphyllum Alkaloids: (+)-Daphlongamine E, (+)-Calyciphylline R, and (–)-10-Deoxydaphnipaxianine A;Synthesis;2024-01-12

2. Total Syntheses of Calyciphylline A-Type Alkaloids (−)-10-Deoxydaphnipaxianine A, (+)-Daphlongamine E and (+)-Calyciphylline R via Late-Stage Divinyl Carbinol Rearrangements;Journal of the American Chemical Society;2022-08-25

3. [3,3]-Sigmatropic rearrangements: a variety of methods and recent advances;Russian Chemical Reviews;2022

4. Microwave‐Assisted 1,3‐Dioxa‐[3,3]‐Sigmatropic Rearrangement of Substituted Allylic Carbamates: Application to the Synthesis of Novel 1,3‐Oxazine‐2,4‐dione Derivatives;European Journal of Organic Chemistry;2021-11-19

5. A General Strategy for the Construction of Calyciphylline A‐Type Alkaloids: Divergent Total Syntheses of (−)‐Daphenylline and (−)‐Himalensine A;Angewandte Chemie International Edition;2021-03-18

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