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Hept-3-ene

The decomposition following FI of variously 13C- and D-labelled hept-1-enes have been studied over the time range from tens of picoseconds... [Pg.108]

HEPTENE or 1-HEPTENE or HEPT-1-ENE or w-HEPTENE 592-16-1 25339-56-4) C7H,4 Highly flammable liquid. Forms explosive mixture with air [explosion limits in air (vol %) 1.0 to uel unkonwn flash point less than 25°F/-4°C autoignition temp500°F/260°C Fire Rating 3]. Reacts... [Pg.534]

The interaction of a alk-l-ene and phosphorus pentachloride to form a complex of the general composition RCH=CH2 2PCl5, now recognized as having the phosphonium salt structure 73, has been known for some time. Very many examples are now known of the decomposition of such complexes with SO2 (or in some cases with P40io ) under controlled conditions when the products are (2-chloroalkyl)phosphonic dichlorides (74) or derivatives thereof. The acids from but-l-ene and pent-l-ene hex-l-ene and hept-1-ene and oct-l-ene and dec-l-ene ° have all been reported. The stability of the initial adducts appears to very considerably, and dehydrochlorination may occur readily if the reaction is carried out with insufficient control. Vinyl and isopropenyl esters of carboxylic... [Pg.161]

Bicyclo[2.1.0]pentane-5-spirocyclopropane, Bicyclo[3.2.0]-hept-1-ene, 5-Methylenebicyclo[2.1.1]hexane, 1,2,6-Heptatriene, 3-Methylene-1,5-hexadiene and Tricyclo[4.1.0.0 ]heptane... [Pg.198]

HT (Z)-trimethyl hept-2-ene-2,4,6-tricarboxylate HT trimethyl hept-1-ene-2,4,6-tncarboxylate... [Pg.97]

An hypothesis known as Bredt s Rule states that a double bond to a bridgehead of a smallring bridged bicyclic compound is not possible. The basis of this rule can be seen if you attempt to make a model of bicyclo[2.2.1 ]hept- 1-ene, A. One approach to the assembly of this model is to try to bridge the number 1 and number 4 carbon atoms of cyclohexene with a methylene (CH2) unit. Compare this bridging with the ease of installing a CH2 bridge... [Pg.688]


See other pages where Hept-3-ene is mentioned: [Pg.817]    [Pg.131]    [Pg.136]    [Pg.412]    [Pg.419]    [Pg.420]    [Pg.429]    [Pg.3273]    [Pg.3313]    [Pg.3533]    [Pg.80]    [Pg.295]    [Pg.171]    [Pg.519]    [Pg.186]    [Pg.492]    [Pg.238]    [Pg.191]    [Pg.191]    [Pg.192]    [Pg.192]    [Pg.192]    [Pg.196]    [Pg.235]    [Pg.344]    [Pg.1384]    [Pg.1384]    [Pg.1384]    [Pg.1384]    [Pg.1607]    [Pg.1607]    [Pg.2169]   


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2-Methyl-2,7-diazabicyclo hept-4-enes

2.2- dihalo-4-azabicyclo hept-5-ene ester

7-Oxabicyclo hept-5-ene

Bicyclo hept-2-ene

Bicyclo hept-2-ene oxidative cleavage

Bicyclo hept-2-ene potassium permanganate

Bicyclo hept-2-enes synthesis

Bicyclo hept-2-enes thermal isomerizations

Bicyclo hept-2-enes via retro Diels-Alder reactions

Bicyclo hept-2-enes, 7- Cope rearrangement

Bicyclo hept-3-ene, 7,7-dichloro

Bicyclo hept-3-enes photoisomerization

Bicyclo hept-3-enes rearrangement

Bicyclo hept-5-enes thermolysis

Bicyclo hept-l-ene

Hept-

Hept-l-ene

PINENE, BICYCL0 HEPT-2-ENE

Poly(2,3-bicyclo hept-2-enes

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