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8-Cyclopentyl-3-

RN 61379-65-5 MF C47H64N40,2 MW 877.05 EINECS 262-743-9 CN 3-[[(4-Cyclopentyl-l-piperazinyl)imino]methyl]rifamycin... [Pg.1812]

There is, no doubt, a decrease in the homoaromatic stabilization when conjugation is interrupted in two (bishomoaromatic) or more places (Paquette et al., 1977a Paquette, 1978). In spite of this, several bishomoaromatic cations have been well characterized. The simplest bishomoaromatic the 4-cyclopentyl cation [29] is, as yet, unknown (see Olah et al., 1972, and references cited therein). The cation [29] was not detected by NMR studies, nor was it invoked as an intermediate in the solvolysis of appropriately substituted cyclopentenes. [Pg.286]

Piperidine, 3-aryloxymethyl-4-phenyl-as antidepressant, 1, 169 Piperidine, N-bromo-photoelectron spectroscopy, 2, 142 Piperidine, cis-4-f-butyl-r-cyclohexyl-l-phenyl-X-ray analysis, 2, 161 Piperidine, 3-chloro-pyrrolidines from, 4, 147 Piperidine, JV-chloro-photoelectron spectroscopy, 2, 142 reactions, 2, 373 trimerization, 3, 510 Piperidine, 4-cyclopentyl-2,6-dioxo-synthesis... [Pg.746]

Chemical Name Rifamycin, 3-(((4-cyclopentyl-l-piperazinyl)imino)methyl)-Common Name Rifapentine... [Pg.2979]

Buten 4-Cyclopentyl-l-hydroxy-EI9a, 761 (C-B-Spaltung/ + Vinyl-Oxiran)... [Pg.663]

The cocrystal structure of 57 with ERa revealed that the more favorable interaction of the 5-OH with His524 compensates for the shift in the position of the D-ring required for binding with SERBA-1. Changing the ring size of the 3,4-cyclopentyl group to a cyclohexyl or cycloheptyl did not have much impact on either ER 3 affinity or selectivity. Attachment of a cyclopentanone (58) or cyclohexanone ring to the 3,4-position increased ERP selectivity to 100- and 40-fold, respectively, but also... [Pg.80]


See other pages where 8-Cyclopentyl-3- is mentioned: [Pg.1813]    [Pg.436]    [Pg.921]    [Pg.1174]    [Pg.732]    [Pg.2352]    [Pg.2352]    [Pg.2353]    [Pg.2353]    [Pg.2353]    [Pg.2353]    [Pg.2353]    [Pg.2353]    [Pg.2353]    [Pg.2353]    [Pg.2353]    [Pg.86]    [Pg.2980]    [Pg.96]    [Pg.1813]    [Pg.436]    [Pg.762]    [Pg.809]    [Pg.1017]    [Pg.1155]    [Pg.1175]    [Pg.20]    [Pg.34]    [Pg.2352]    [Pg.2352]    [Pg.2353]    [Pg.2353]    [Pg.2353]    [Pg.2353]   
See also in sourсe #XX -- [ Pg.921 , Pg.1220 ]




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1-Cyclopentyl-5-nitro

16-Cyclopentyl-17,20-tetranor

2- cyclopentyl phenyl

2-Cyclopentyl-cyclopentanone

3-cyclopentyl ether

9-Cyclopentyl-9-borabarbaralane

Alcohol cyclopentyl secondary

CPME (Cyclopentyl methyl ether

Comparison of Cyclopentyl and Norbornyl Derivatives

Cyclobutylcarbinyl —cyclopentyl

Cyclohexyl-cyclopentyl

Cyclopentyl Annulations via Vinylcyclopropanes

Cyclopentyl Synthesis

Cyclopentyl acetate

Cyclopentyl acetate, hydrolysis

Cyclopentyl aldehyde

Cyclopentyl anions

Cyclopentyl azide

Cyclopentyl benzoate

Cyclopentyl bromide

Cyclopentyl bromide, reaction

Cyclopentyl carbinol

Cyclopentyl carbocation

Cyclopentyl carbocation rearrangement

Cyclopentyl cation

Cyclopentyl cation 1,2-hydride shift

Cyclopentyl chloride

Cyclopentyl chloride, reaction

Cyclopentyl cyanide

Cyclopentyl ethyl ether

Cyclopentyl fluorides

Cyclopentyl group

Cyclopentyl iodide

Cyclopentyl iodide, reaction

Cyclopentyl magnesium chloride

Cyclopentyl methyl ether

Cyclopentyl methyl ketone

Cyclopentyl radicals

Cyclopentyl radicals, reactions

Cyclopentyl ring

Ethynyl estradiol 3-cyclopentyl

Ketones cyclopentyl

N-Cyclopentyl

O-Cyclopentyl S-

Protection cyclopentyl esters

Rearrangement cyclobutylcarbinyl—cyclopentyl

Sulfones, cyclopentyl

Viridenomycin, cyclopentyl core

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