| Enes obliquus | |
|---|---|
Scientific classification  | |
| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Arthropoda |
| Class: | Insecta |
| Order: | Coleoptera |
| Infraorder: | Cucujiformia |
| Family: | Cerambycidae |
| Subfamily: | Lamiinae |
| Genus: | Enes |
| Species: | E. obliquus |
| Binomial name | |
| Enes obliquus Pascoe, 1864 | |
Enes obliquus is a species of beetle in the family Cerambycidae. It was described by Pascoe in 1864. [1]
In organic chemistry, a group transfer reaction is a class of the pericyclic reaction where one or more groups of atoms is transferred from one molecule to another. Group transfer reactions can sometimes be difficult to identify when separate reactant molecules combine into a single product molecule. Unlike other pericyclic reaction classes, group transfer reactions do not have a specific conversion of pi bonds into sigma bonds or vice versa, and tend to be less frequently encountered. Like all pericyclic reactions, group transfer reactions must obey the Woodward–Hoffmann rules. Group transfer reactions can be divided into two distinct subcategories: the ene reaction and the diimide reduction. Group transfer reactions have diverse applications in various fields, including protein adenylation, biocatalytic and chemoenzymatic approaches for chemical synthesis, and strengthening skim natural rubber latex.
In organic chemistry, the ene reaction is a chemical reaction between an alkene with an allylic hydrogen and a compound containing a multiple bond, in order to form a new σ-bond with migration of the ene double bond and 1,5 hydrogen shift. The product is a substituted alkene with the double bond shifted to the allylic position.
In organic chemistry, hexene is a hydrocarbon with the chemical formula C6H12. The prefix "hex" is derived from the fact that there are 6 carbon atoms in the molecule, while the "-ene" suffix denotes that there is an alkene present—two carbon atoms are connected via a double bond. There are several isomers of hexene, depending on the position and geometry of the double bond in the chain. One of the most common industrially useful isomers is 1-hexene, an alpha-olefin. Hexene is used as a comonomer in the production of polyethylene.
But-2-ene is an acyclic alkene with four carbon atoms. It is the simplest alkene exhibiting cis/trans-isomerism (also known as (E/Z)-isomerism); that is, it exists as two geometric isomers cis-but-2-ene ((Z)-but-2-ene) and trans-but-2-ene ((E)-but-2-ene).
Androstenediol, or 5-androstenediol, also known as androst-5-ene-3β,17β-diol, is an endogenous weak androgen and estrogen steroid hormone and intermediate in the biosynthesis of testosterone from dehydroepiandrosterone (DHEA). It is closely related to androstenedione (androst-4-ene-3,17-dione).
EcoHomes was an environmental rating scheme for homes in the United Kingdom. It was the domestic version of the Building Research Establishment's Environmental Assessment Method BREEAM, which could also be applied to a variety of non-residential buildings. It was replaced by the Code for Sustainable Homes in April 2008.
In enzymology, a 24-hydroxycholesterol 7alpha-hydroxylase (EC 1.14.13.99) is an enzyme that catalyzes the chemical reaction
Enes Kanter Freedom is an American professional basketball player and human rights activist who last played for the Boston Celtics of the National Basketball Association (NBA). He also had a brief professional wrestling career, where he is a former WWE 24/7 Champion. Born in Switzerland to Turkish parents, he was raised in Turkey and moved to the United States as a teenager. Freedom was selected as the third overall pick of the 2011 NBA draft by the Utah Jazz. A center, Freedom played for five NBA teams during his eleven-year career.
Alexandru Ene was a Romanian football striker.
Gheorghe Ene was a Romanian football striker and coach.
1-Androstenedione, or 5α-androst-1-ene-3,17-dione, also known as 4,5α-dihydro-δ1-4-androstenedione, is a synthetic androgen and anabolic steroid. It is a 5α-reduced isomer of the endogenous steroid 4-androstenedione and acts as an androgen prohormone of 1-testosterone (4,5α-dihydro-δ1-testosterone), a derivative of dihydrotestosterone (DHT).
Enes Ünal is a Turkish professional footballer who plays as a forward for Premier League club Bournemouth and the Turkey national team.
The 17th Robert Awards ceremony was held in 2000 in Copenhagen, Denmark. Organized by the Danish Film Academy, the awards honoured the best in Danish and foreign film of 1999.
7α-Methyl-19-norandrostenedione, or 7α-methyl-19-norandrost-4-ene-3,17-dione, also known as trestione, as well as 7α-methylestr-4-ene-3,17-dione, is a synthetic anabolic-androgenic steroid (AAS) and a derivative of 19-nortestosterone (nandrolone). It may act as a prohormone of trestolone. MENT dione has been sold on the Internet under the name Mentabolan as a "dietary supplement".
Androstenediol 17β-acetate, or 5-androstenediol 17β-acetate, also known as androst-5-ene-3β,17β-diol 17β-acetate, is a synthetic anabolic-androgenic steroid and an androgen ester – specifically, the C17β acetate ester of 5-androstenediol (androst-5-ene-3β,17β-diol) – which was never marketed.
Androstenediol 3β-acetate, or 5-androstenediol 3β-acetate, also known as androst-5-ene-3β,17β-diol 3β-acetate, is a synthetic anabolic-androgenic steroid and an androgen ester – specifically, the C3β acetate ester of 5-androstenediol (androst-5-ene-3β,17β-diol) – which was never marketed.
In organic chemistry, the Myers allene synthesis is a chemical reaction that converts a propargyl alcohol into an allene by way of an arenesulfonylhydrazine as a key intermediate. This name reaction is one of two discovered by Andrew Myers that are named after him; both this reaction and the Myers deoxygenation reaction involve the same type of intermediate.
Vizcatán del Ene district is one of the nine constituent districts of Satipo Province situated in the eastern part of the Department of Junín, Peru.
In organic chemistry, the Conia-ene reaction is an intramolecular cyclization reaction between an enolizable carbonyl such as an ester or ketone and an alkyne or alkene, giving a cyclic product with a new carbon-carbon bond. As initially reported by J. M. Conia and P. Le Perchec, the Conia-ene reaction is a heteroatom analog of the ene reaction that uses an enol as the ene component. Like other pericyclic reactions, the original Conia-ene reaction required high temperatures to proceed, limiting its wider application. However, subsequent improvements, particularly in metal catalysis, have led to significant expansion of reaction scope. Consequently, various forms of the Conia-ene reaction have been employed in the synthesis of complex molecules and natural products.