Evidence map›Paper›PMID 35495485›Full record

ReviewRSC advances2021

Direct synthesis of sulfenamides, sulfinamides, and sulfonamides from thiols and amines.

Yan Cao, Shahrzad Abdolmohammadi, Roya Ahmadi, Alibek Issakhov, Abdol Ghaffar Ebadi, Esmail Vessally

Open access · goldAbstract readReview
In one paragraph

Review in RSC advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.1field-weighted citation impact, top 7% of its field
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

8 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Synthesis ofSynthesis · 2023
    Article
  7. Review
  8. Review
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

6 authors at 5 institutions in 3 countries.

Yan CaoSchool of Mechatronic Engineering, Xi'an Technological University Xi'an 710021 China.
Shahrzad AbdolmohammadiDepartment of Chemistry, South Tehran Branch, Islamic Azad University P.O. Box 11365-4435 Tehran Iran s.abdolmohamadi@iauet.ac.ir.ORCID https://orcid.org/0000-0001-8187-9624
Roya AhmadiDepartment of Chemistry, College of Basic Sciences, Yadegar-e-Imam Khomeini (RAH) Shahre Rey Branch, Islamic Azad University Tehran Iran.
Alibek IssakhovDepartment of Mathematical and Computer Modelling, Al-Farabi Kazakh National University Almaty 050040 Kazakhstan.
Abdol Ghaffar EbadiDepartment of Agriculture, Jouybar Branch, Islamic Azad University Jouybar Iran.
Esmail VessallyDepartment of Chemistry, Payame Noor University P. O. Box 19395-3697 Tehran Iran.ORCID https://orcid.org/0000-0002-6465-7605
Islamic Azad University, Tehran · IRIslamic Azad University South Tehran Branch · IRKazakh-British Technical University · KZPayame Noor University · IRXi'an Technological University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Needless to say that organosulfur compounds with sulfur-nitrogen bonds have found various applications in diverse fields such as pharmaceuticals, agrochemicals, polymers, and so forth. Three major groups of such compounds are sulfenamides, sulfinamides, and sulfonamides which have been widely applied as building blocks in medical chemistry. Owing to their significant role in drug design and discovery programs, the search for and development of efficient, environmentally friendly, and economic processes for the preparation of the title compounds is of great importance in the pharmaceutical industry. Recently, oxidative coupling of thiols and amines, two readily available low-cost commodity chemicals, has emerged as a highly useful method for synthesizing structurally diverse sulfenamides, sulfinamides, and sulfonamides in a single step. Since this strategy does not require additional pre-functionalization and de-functionalization steps, it considerably streamlines synthetic routes and substantially reduces waste generation. This review will focus on recent advances and achievements in this attractive research arena.

Identifiers

PMID35495485
PMCPMC9042206
OpenAlexW3203385049

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.