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cyclopropane's Usage Examples:

In enzymology, a cyclopropane-fatty-acyl-phospholipid synthase (EC 2.

analogously to their normal alkane counterparts of the same carbon count: cyclopropane, cyclobutane, cyclopentane, cyclohexane, etc.

Cyclopropanation refers to any chemical process which generates cyclopropane rings.

resembling a similar "bent" structure within small ring molecules, such as cyclopropane (C3H6) or as a representation of double or triple bonds within a compound.

The simplest alicyclic compounds are the monocyclic cycloalkanes: cyclopropane, cyclobutane, cyclopentane, cyclohexane, cycloheptane, cyclooctane, and.

Strain is most commonly discussed for small rings such as cyclopropanes and cyclobutanes, whose internal angles are substantially smaller than.

The systematic name of this enzyme class is cycloeucalenol lyase (cyclopropane-decyclizing).

the product resulting from the electrophilic addition of water to the cyclopropane moiety of synthetic cannabinoid UR-144.

colorless gas is the monomethyl derivative of cyclopropane.

Methylcyclopropane, like many other cyclopropanes, undergoes ring-opening reactions.

(ACC) is a disubstituted cyclic α-amino acid in which a three-membered cyclopropane ring is fused to the Cα atom of the amino acid.

An equivalent hydrate hexahydroxycyclopropane or cyclopropane-1,1,2,2,3,3-hexol, (-C(OH)2-)3 also exists.

the cyclopropane ring and the cis-configuration at the olefinic carbon-carbon double bond and 8% of the isomer with cis geometry on the cyclopropane ring.

Cyclopropane fatty acids (CPA) are a subgroup of fatty acids that contain a cyclopropane group.

It has a strained ring system with a cyclopentane ring fused to a cyclopropane ring.

In organometallic chemistry, the activation of cyclopropanes by transition metals is a research theme with implications for organic synthesis and homogeneous.

3-Carene is a bicyclic monoterpene consisting of fused cyclohexene and cyclopropane rings.

Methylenecyclopropane is an organic compound with the formula (CH2)2CCH2.

rearrangement is an organic reaction for converting a geminal dihalo cyclopropane to an allene using an organolithium base.

cyclopropane's Meaning':

a colorless flammable gas sometimes used as an inhalation anesthetic