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REACTION OF SUBSTITUTED SPIRO[1,2,3,4-TETRAHYDRONAPHTHALENE-2,3’-(1’- PYRAZOLINES)] WITH CHLORINATING REAGENTS. / Molchanov, A.P.; Korotkov, V.S.; Kostikov, R.R.

в: Russian Journal of Organic Chemistry, № 8, 2006, стр. 1146-1150.

Результаты исследований: Научные публикации в периодических изданиях › статья

Harvard

Molchanov, AP, Korotkov, VS & Kostikov, RR 2006, 'REACTION OF SUBSTITUTED SPIRO[1,2,3,4-TETRAHYDRONAPHTHALENE-2,3’-(1’- PYRAZOLINES)] WITH CHLORINATING REAGENTS', Russian Journal of Organic Chemistry, № 8, стр. 1146-1150. <http://elibrary.ru/item.asp?id=12018579>

APA

Molchanov, A. P., Korotkov, V. S., & Kostikov, R. R. (2006). REACTION OF SUBSTITUTED SPIRO[1,2,3,4-TETRAHYDRONAPHTHALENE-2,3’-(1’- PYRAZOLINES)] WITH CHLORINATING REAGENTS. Russian Journal of Organic Chemistry, (8), 1146-1150. http://elibrary.ru/item.asp?id=12018579

Vancouver

Molchanov AP, Korotkov VS, Kostikov RR. REACTION OF SUBSTITUTED SPIRO[1,2,3,4-TETRAHYDRONAPHTHALENE-2,3’-(1’- PYRAZOLINES)] WITH CHLORINATING REAGENTS. Russian Journal of Organic Chemistry. 2006;(8):1146-1150.

Author

Molchanov, A.P. ; Korotkov, V.S. ; Kostikov, R.R. / REACTION OF SUBSTITUTED SPIRO[1,2,3,4-TETRAHYDRONAPHTHALENE-2,3’-(1’- PYRAZOLINES)] WITH CHLORINATING REAGENTS. в: Russian Journal of Organic Chemistry. 2006 ; № 8. стр. 1146-1150.

BibTeX

@article{a2695778626440c2a0af3517eadc490b,
title = "REACTION OF SUBSTITUTED SPIRO[1,2,3,4-TETRAHYDRONAPHTHALENE-2,3{\textquoteright}-(1{\textquoteright}- PYRAZOLINES)] WITH CHLORINATING REAGENTS",
abstract = "In reaction of 4{\textquoteright}-arylspiro[1,2,3,4-tetrahydronaphthalene-2,3{\textquoteright}-(1{\textquoteright}- pyrazolin)]-1-ones with N-chlorosuccinimide formed spirocyclic substituted 3-chloro-1-pyrazolines that lost nitrogen at heating transforming into spirocyclic chlorocyclopropanes. The reaction of the same pyrazolines with chlorine led to the formation of spirocyclic gem-dichlorocyclopropanes. {\textcopyright} Nauka/Interperiodica 2006.",
author = "A.P. Molchanov and V.S. Korotkov and R.R. Kostikov",
year = "2006",
language = "English",
pages = "1146--1150",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "8",

}

RIS

TY - JOUR

T1 - REACTION OF SUBSTITUTED SPIRO[1,2,3,4-TETRAHYDRONAPHTHALENE-2,3’-(1’- PYRAZOLINES)] WITH CHLORINATING REAGENTS

AU - Molchanov, A.P.

AU - Korotkov, V.S.

AU - Kostikov, R.R.

PY - 2006

Y1 - 2006

N2 - In reaction of 4’-arylspiro[1,2,3,4-tetrahydronaphthalene-2,3’-(1’- pyrazolin)]-1-ones with N-chlorosuccinimide formed spirocyclic substituted 3-chloro-1-pyrazolines that lost nitrogen at heating transforming into spirocyclic chlorocyclopropanes. The reaction of the same pyrazolines with chlorine led to the formation of spirocyclic gem-dichlorocyclopropanes. © Nauka/Interperiodica 2006.

AB - In reaction of 4’-arylspiro[1,2,3,4-tetrahydronaphthalene-2,3’-(1’- pyrazolin)]-1-ones with N-chlorosuccinimide formed spirocyclic substituted 3-chloro-1-pyrazolines that lost nitrogen at heating transforming into spirocyclic chlorocyclopropanes. The reaction of the same pyrazolines with chlorine led to the formation of spirocyclic gem-dichlorocyclopropanes. © Nauka/Interperiodica 2006.

M3 - Article

SP - 1146

EP - 1150

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 8

ER -

ID: 5018495