cyclopropane$18427$ - definition. What is cyclopropane$18427$
Diclib.com
قاموس ChatGPT
أدخل كلمة أو عبارة بأي لغة 👆
اللغة:

ترجمة وتحليل الكلمات عن طريق الذكاء الاصطناعي ChatGPT

في هذه الصفحة يمكنك الحصول على تحليل مفصل لكلمة أو عبارة باستخدام أفضل تقنيات الذكاء الاصطناعي المتوفرة اليوم:

  • كيف يتم استخدام الكلمة في اللغة
  • تردد الكلمة
  • ما إذا كانت الكلمة تستخدم في كثير من الأحيان في اللغة المنطوقة أو المكتوبة
  • خيارات الترجمة إلى الروسية أو الإسبانية، على التوالي
  • أمثلة على استخدام الكلمة (عدة عبارات مع الترجمة)
  • أصل الكلمة

%ما هو (من)٪ 1 - تعريف

CHEMICAL PROCESS WHICH GENERATES CYCLOPROPANE RINGS
Kishner cyclopropane synthesis
  • 400px
  • 600px
  • 500px
  • Structure of U-106305, a derivative of a [[cyclopropane fatty acid]] with six cyclopropane rings, isolated from ''Streptomyces sp''

Cyclopropane-fatty-acyl-phospholipid synthase         
CLASS OF ENZYMES
EC 2.1.1.79; S-adenozil-L-metionin:unsaturated-phospholipid methyltransferase (cyclizing)
In enzymology, a cyclopropane-fatty-acyl-phospholipid synthase () is an enzyme that catalyzes the chemical reaction
Activation of cyclopropanes by transition metals         
  • 495x495px
  • 459x459px
  • 367x367px
  • 447x447px
  • 553x553px
  • 553x553px
  • 558x558px
  • Oxidative addition into cyclopropane C-C bond gives a metallacyclobutane.
  • 434x434px
  • 445x445px
  • 517x517px
  • 702x702px
  • 500x500px
Cyclopropane C-C Activation; Cyclopropane carbon-carbon bond activation
In organometallic chemistry, the activation of cyclopropanes by transition metals is a research theme with implications for organic synthesis and homogeneous catalysis. Being highly strained, cyclopropanes are prone to oxidative addition to transition metal complexes.
Trimethylene         
  • Orbital overlap in the bent bonding model of cyclopropane
CHEMICAL COMPOUND
Cyclopropanes; Freund reaction; Trimethylene; Cyclolpropane
·noun A gaseous hydrocarbon, C3H6, isomeric with propylene and obtained from it indirectly. It is the base of a series of compounds analogous to the aromatic hydrocarbons.

ويكيبيديا

Cyclopropanation

In organic chemistry, cyclopropanation refers to any chemical process which generates cyclopropane ((CH2)3) rings. It is an important process in modern chemistry as many useful compounds bear this motif; for example pyrethroids and a number of quinolone antibiotics (ciprofloxacin, sparfloxacin, etc.). However, the high ring strain present in cyclopropanes makes them challenging to produce and generally requires the use of highly reactive species, such as carbenes, ylids and carbanions. Many of the reactions proceed in a cheletropic manner.