Статьи из солнечного Азербайджана

[VOVAN CIR]

Коллеги, добрый день!

Если есть у кого возможность, помогите, пожалуйста, добыть статьи:

1) +++

2) Mamedov, M. K.; Gadzhieva, I. N. Azerbaidzhanskii Khimicheskii Zhurnal (2002), (2), 56-60.

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5) Mammadov, M. K. Azarbaycan Neft Tasarrufati (2012), (11), 48-54.

Спасибо.

[sveta]

выполнено
3) Musaev, D. D.; Abbasov, M. M.; Sultanov, S. A.; Abbaov, V. A.; Magarlamov, G. Kh. Azerbaidzhanskii Khimicheskii Zhurnal (1998), (4), 101-105.

[VOVAN CIR]

sveta,

Спасибо большое!

[Ol.Lo]

VOVAN CIR, укажите источник, откуда появился запрос под номером 5.
Не получается найти журнал.

[mishka]

в скайфандере есть такая библиография (без указания номера журнала)
Synthesis of cyclohexylnorbornane and its methyl-substituted derivatives. Mammadov, M. K. Inst. of Petrochem. Processes, Azerbaijan. Azarb. Neft Tasarrufati (2012), 48-54. Publisher: (Azarbaycan Neft Tasarrufati, ) CODEN:AZNKAY ISSN:0365-8554. Journal written in Russian. CAN 160:530307 AN 2013:1485810 CAPLUS

ABSTRACT Different initiators: combination reactions of norbornene and Me norbornene to cyclohexane and methylcyclohexane was studied with contribution of benzoyl peroxide, azo-bis-isobutyric acid dinitrile and bis(t-butyl)peroxide. Cyclohexylnorbornane and its Me derivations were synthesized in 71.9-78.5% yields using the most effective initiator bis(t-butyl)peroxide. The synthesized norbornanes exist as endo- and exo-isomers. The isomer mixt. was heated in a digester at 200-210° and it was turned only into exo-isomer. Phys.-chem. characteristics of synthesized substances were studied, their structure was confirmed and at the result hydrocarbons with high d. and energy were synthesized. Results indicated that synthesized cyclohexylnorbornanes may be used in reactive fuels.

[Ol.Lo]

Хорошо. Поищу ещё раз.

[Ol.Lo]

Оригинал не найден.