Published June 1999
| Version v1
Journal article
Synthesis of 1-primary alkylamino-o-carboranes by reduction of 1-primary alkylnitro-o-carboranes
- 1. RAN, Inst. Ehlementorganicheskikh Soedinenij im. A.N. Nesmeyanova, Moscow (Russian Federation)
Description
By action of 1-sodium-o-carboranes in liquid ammonia on α,β-unsaturated nitro compounds an easy addition of 1-sodium-o-carboranes to 1-4 positions of α,β-unsaturated nitro compounds is observed resulting in o-carborane nitro derivatives. Primary alkylamino-o-carboranes isolated as a hydrochlorides have been prepared by reducing some o-carborane nitro derivatives with LiAlH4 in ether solutions
Abstract (Russian)
При действии 1-натрий-о-карборанов в жидком аммиаке на α,β-непредельные нитросоединения легко происходит присоединение 1--натрий-о-карборанов в положение 1-4 α,β-непредельного нитросоединения с образованием нитропроизводных о-карборанов. Восстановлением некоторых нитропроизводных о-карборанов с использованием LiAlH4 в эфирном растворе получены первичные алкилоамино-о-карбораны, выделенные в виде гидрохлоридовAdditional details
Additional titles
- Original title (Russian)
- Синтез 1-первичных алкиламино-о-карборанов восстановлением 1-первичных алкилнитро-о-карборанов
Publishing Information
- Journal Title
- Zhurnal Obshchej Khimii
- Journal Volume
- 69
- Journal Issue
- 6
- Journal Page Range
- p. 954-956
- ISSN
- 0044-460X
- CODEN
- ZOKHA4
INIS
- Country of Publication
- Russian Federation
- Country of Input or Organization
- Russian Federation
- INIS RN
- 31036986
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- AMINES; AMMONIA; CARBORANES; CHEMICAL COMPOSITION; CHEMICAL PREPARATION; CHEMICAL REACTION YIELD; INFRARED SPECTRA; NITRO COMPOUNDS; REDUCTION
- Descriptors DEC
- CARBON COMPOUNDS; CHEMICAL REACTIONS; HYDRIDES; HYDROGEN COMPOUNDS; NITROGEN COMPOUNDS; NITROGEN HYDRIDES; ORGANIC BORON COMPOUNDS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; SPECTRA; SYNTHESIS; YIELDS
Optional Information
- Notes
- 5 refs.