Tetrahedron Letters, volume 48, issue 39, pages 6890-6892

An efficient synthesis of 1-H indazoles

P D Lokhande ¹

Abdul Raheem ¹

S T Sabale ¹

A R Chabukswar ¹

S C Jagdale ¹

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The Center for Advanced Studies, Department of Chemistry, University of Pune, Pune 411 007, India |

Publication type: Journal Article

Publication date: 2007-09-01

Elsevier

Journal: Tetrahedron Letters

Quartile SCImago

Quartile WOS

Impact factor: 1.8

ISSN: 00404039, 18733581

DOI: 10.1016/j.tetlet.2007.07.162

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Organic Chemistry

Drug Discovery

Biochemistry

Abstract

The reaction of substituted salicyaldehydes with hydrazine hydrochloride under different conditions gave the corresponding 1-H indazoles. However, the reaction of benzaldehydes with hydrazine hydrate under the same conditions yielded only hydrazones.

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Tetrahedron	Tetrahedron, 2, 7.69% Tetrahedron 2 publications, 7.69%
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Organic Preparations and Procedures International	Organic Preparations and Procedures International, 2, 7.69% Organic Preparations and Procedures International 2 publications, 7.69%
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Green Chemistry	Green Chemistry, 1, 3.85% Green Chemistry 1 publication, 3.85%
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ChemInform	ChemInform, 1, 3.85% ChemInform 1 publication, 3.85%
Journal of Organic Chemistry	Journal of Organic Chemistry, 1, 3.85% Journal of Organic Chemistry 1 publication, 3.85%
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Current Organocatalysis	Current Organocatalysis, 1, 3.85% Current Organocatalysis 1 publication, 3.85%
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Citations by publishers

	1 2 3 4 5 6 7 8 9
Elsevier	Elsevier, 9, 34.62% Elsevier 9 publications, 34.62%
Wiley	Wiley, 4, 15.38% Wiley 4 publications, 15.38%
American Chemical Society (ACS)	American Chemical Society (ACS), 4, 15.38% American Chemical Society (ACS) 4 publications, 15.38%
Springer Nature	Springer Nature, 2, 7.69% Springer Nature 2 publications, 7.69%
Taylor & Francis	Taylor & Francis, 2, 7.69% Taylor & Francis 2 publications, 7.69%
Multidisciplinary Digital Publishing Institute (MDPI)	Multidisciplinary Digital Publishing Institute (MDPI), 1, 3.85% Multidisciplinary Digital Publishing Institute (MDPI) 1 publication, 3.85%
Royal Society of Chemistry (RSC)	Royal Society of Chemistry (RSC), 1, 3.85% Royal Society of Chemistry (RSC) 1 publication, 3.85%
Bentham Science	Bentham Science, 1, 3.85% Bentham Science 1 publication, 3.85%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii	Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii, 1, 3.85% Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii 1 publication, 3.85%
	1 2 3 4 5 6 7 8 9

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GOST Copy

Lokhande P. D. et al. An efficient synthesis of 1-H indazoles // Tetrahedron Letters. 2007. Vol. 48. No. 39. pp. 6890-6892.

GOST all authors (up to 50) Copy

Lokhande P. D., Raheem A., Sabale S. T., Chabukswar A. R., Jagdale S. C. An efficient synthesis of 1-H indazoles // Tetrahedron Letters. 2007. Vol. 48. No. 39. pp. 6890-6892.

RIS |

Cite this

RIS Copy

TY - JOUR

DO - 10.1016/j.tetlet.2007.07.162

UR - https://doi.org/10.1016/j.tetlet.2007.07.162

TI - An efficient synthesis of 1-H indazoles

T2 - Tetrahedron Letters

AU - Lokhande, P D

AU - Raheem, Abdul

AU - Sabale, S T

AU - Chabukswar, A R

AU - Jagdale, S C

PY - 2007

DA - 2007/09/01 00:00:00

PB - Elsevier

SP - 6890-6892

IS - 39

VL - 48

SN - 0040-4039

SN - 1873-3581

ER -

BibTex |

Cite this

BibTex Copy

@article{2007_Lokhande,

author = {P D Lokhande and Abdul Raheem and S T Sabale and A R Chabukswar and S C Jagdale},

title = {An efficient synthesis of 1-H indazoles},

journal = {Tetrahedron Letters},

year = {2007},

volume = {48},

publisher = {Elsevier},

month = {sep},

url = {https://doi.org/10.1016/j.tetlet.2007.07.162},

number = {39},

pages = {6890--6892},

doi = {10.1016/j.tetlet.2007.07.162}

}

MLA

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MLA Copy

Lokhande, P. D., et al. “An efficient synthesis of 1-H indazoles.” Tetrahedron Letters, vol. 48, no. 39, Sep. 2007, pp. 6890-6892. https://doi.org/10.1016/j.tetlet.2007.07.162.

Found error?

Publisher

Elsevier

Journal

Tetrahedron Letters

Quartile SCImago

Quartile WOS

Impact factor

1.8

ISSN

00404039 (Print)
18733581 (Electronic)