Evidence map›Paper›PMID 23390951›Full record

ArticleJournal of the American Chemical Society2013

A catalytic enantioselective tandem allylation strategy for rapid terpene construction: application to the synthesis of pumilaside aglycon.

Grace E Ferris, Kai Hong, Ian A Roundtree, James P Morken

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Transition-Metal-Free Borylation of Allylic and Propargylic Alcohols.Angewandte Chemie (International ed. in English) · 2016
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

4 authors.

Grace E FerrisDepartment of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, USA.
Kai Hong
Ian A Roundtree
James P Morken

Funding

DEVELOPMENT AND STUDY OF ENZYME FUNCTIONAL MIMICSR01GM059417 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MORKEN, JAMES PATRICK · 1999 to 2017
$4.1M
STRUCTURE AND MECHANISMS OF FAMILY 18 CHITINASESR01GM059471 · NIGMS · DUQUESNE UNIVERSITY · PI MADURA, JEFFRY D. · 1998 to 2002
$642k
Development of Catalytic Conjunctive Coupling ReactionsR01GM118641 · NIGMS · BOSTON COLLEGE · PI MORKEN, JAMES PATRICK · 2017 to 2018
$635k
NIGMS NIH HHS GM-59471NIGMS NIH HHS R01 GM059417NIGMS NIH HHS R01 GM118641
6 · The paper itself

Abstract

Catalytic enantioselective 1,2-diboration of 1,3-dienes followed by cascade allylborations with dicarbonyls provides rapid entry into carbocyclic reaction products. The stereochemical course of this reaction was studied along with its application in the synthesis of pumilaside aglycon.

Indexed as

Allyl CompoundsCatalysisMolecular StructureSesquiterpenesStereoisomerismTerpenesTime FactorsAllyl CompoundsSesquiterpenesTerpenes

Identifiers

PMID23390951
PMCPMC3625973

What OpenQuestion holds

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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.