The Rich Chemistry Resulting from the 1,3-Dipolar Cycloaddition Reactions of Enamines and Azides

Vasiliy A. Bakulev, Tetyana Beryozkina, Joice Thomas, Wim Dehaen

Research output: Contribution to journalReview articleResearchpeer-review

22 Citations (Scopus)
Original languageEnglish
Pages (from-to)262-294
Number of pages33
JournalEuropean Journal of Organic Chemistry
Volume2018
Issue number3
DOIs
Publication statusPublished - 23 Jan 2018

Fingerprint

Azides
Cycloaddition
cycloaddition
chemistry
Amidines
Triazoles
Stabilization
Derivatives
products
reactivity
stabilization
rings

Keywords

  • Amidines
  • Azides
  • Cycloaddition
  • Enamines
  • Reaction mechanisms
  • Triazoles

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

WoS ResearchAreas Categories

  • Chemistry, Organic

Cite this

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title = "The Rich Chemistry Resulting from the 1,3-Dipolar Cycloaddition Reactions of Enamines and Azides",
keywords = "Amidines, Azides, Cycloaddition, Enamines, Reaction mechanisms, Triazoles",
author = "Bakulev, {Vasiliy A.} and Tetyana Beryozkina and Joice Thomas and Wim Dehaen",
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The Rich Chemistry Resulting from the 1,3-Dipolar Cycloaddition Reactions of Enamines and Azides. / Bakulev, Vasiliy A.; Beryozkina, Tetyana; Thomas, Joice; Dehaen, Wim.

In: European Journal of Organic Chemistry, Vol. 2018, No. 3, 23.01.2018, p. 262-294.

Research output: Contribution to journalReview articleResearchpeer-review

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T1 - The Rich Chemistry Resulting from the 1,3-Dipolar Cycloaddition Reactions of Enamines and Azides

AU - Bakulev, Vasiliy A.

AU - Beryozkina, Tetyana

AU - Thomas, Joice

AU - Dehaen, Wim

PY - 2018/1/23

Y1 - 2018/1/23

KW - Amidines

KW - Azides

KW - Cycloaddition

KW - Enamines

KW - Reaction mechanisms

KW - Triazoles

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U2 - 10.1002/ejoc.201701031

DO - 10.1002/ejoc.201701031

M3 - Review article

VL - 2018

SP - 262

EP - 294

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

SN - 1434-193X

IS - 3

ER -