Evidence map›Paper›PMID 29417970›Full record

ReviewNatural product reports2018

Total synthesis of complex terpenoids employing radical cascade processes.

Kevin Hung, Xirui Hu, Thomas J Maimone

Abstract readReview
In one paragraph

Review in Natural product reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed.

  1. Evolution of a Synthetic Strategy for Complex Diterpenes fromJournal of the American Chemical Society · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. A Mechanistic Investigation of theThe Journal of organic chemistry · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Practical and General Alcohol Deoxygenation Protocol.Angewandte Chemie (International ed. in English) · 2023
    Article
  11. Review
  12. A Photoenzyme for Challenging Lactam Radical Cyclizations.Synlett : accounts and rapid communications in synthetic organic chemistry · 2022
    Article
  13. Convergent total synthesis of (+)-calcipotriol: A scalable, modular approach to vitamin D analogs.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  14. Total syntheses of strained polycyclic terpenes.Chemical communications (Cambridge, England) · 2022
    Review
  15. Article
  16. Bifunctional Polyene Cyclizations: Synthetic Studies on Pimarane Natural Products.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021
    Article
  17. Article
  18. Article
  19. Activation modes in biocatalytic radical cyclization reactions.Journal of industrial microbiology & biotechnology · 2021
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Kevin HungDepartment of Chemistry, University of California - Berkeley, Berkeley, CA 94720, USA. maimone@berkeley.edu.
Xirui Hu
Thomas J Maimone

Funding

Synthesis of Complex Terpenes From Simple Precursors: RenewalR01GM116952 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI MAIMONE, THOMAS JOHN · 2016 to 2024
$2.7M
NIGMS NIH HHS R01 GM116952
6 · The paper itself

Abstract

Covering: 2011-2017Radical cyclizations have a rich history in organic chemistry and have been particularly generous to the field of natural product synthesis. Owing to their ability to operate in highly congested molecular quarters, and with significant functional group compatibility, these transformations have enabled the synthesis of numerous polycyclic terpenoid natural products over the past several decades. Moreover, when programmed accordingly into a synthetic plan, radical cascade processes can be used to rapidly assemble molecular complexity, much in the same way nature rapidly constructs terpene frameworks through cationic cyclization pathways. This review highlights recent total syntheses of complex terpenoids (from 2011-2017) employing C-C bond-forming radical cascade sequences.

Indexed as

Biological ProductsCyclizationDiterpenesDiterpenes, KauraneLimoninsPleuromutilinsPolycyclic CompoundsSesquiterpenesTerpenesBiological ProductscrotogoudinDiterpenesDiterpenes, KauranejiadifeninlimoninLimoninslongikaurin EPleuromutilinsPolycyclic CompoundsSesquiterpenesTerpenes

Identifiers

PMID29417970
PMCPMC5858714

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.