After the alkylation, you may need to dehydrate the resulting compound to form a cyclopentene ring. This can be achieved through the use of acid-catalyzed elimination reactions.
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(7R,8R,9R)-9-benzoyloxy-7,8-dihydroxy-1,4-dithiaspiro<4.5>decane
(7R,8R,9R)-9-benzoyloxy-7,8-dihydroxy-1,4-dithiaspiro<4.5>decane
methyl (E)-2,3-di-O-benzyl-6,7-dideoxy-4-O-(4-methoxybenzyl)-α-D-galacto-oct-6-enoside
C14H10FNOS
9H-Purine, 6-chloro-9-[(4-methylphenyl)methyl]-2-(trifluoromethyl)-
anhydrolevuglandin E2
trans-2-octadecene
cis-1',3'-O-benzylidene-2'-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)glycerol
(2S,3R,4R)-2-(hydroxymethyl)tetrahydrofuran-3,4-diol
(4-cyclohexylbut-1-en-3-yn-2-yl)benzene
5-Cyano-2-hydroxy-2-methyl-4-(2-nitro-phenyl)-6-pyrrolidin-1-yl-1,2,3,4-tetrahydro-pyridine-3-carboxylic acid methyl ester
6,6-dimethyl-2-(5-O-tosyl-α-D-arabinofuranosyl)-4,5,6,7-tetrahydroindol-4-one
1-METHOXY-1-METHYLAMINO-2-NITROETHYLENE
[5-chloro-2-di(5-methyl-2-furyl)methylphenyl](4-methylphenyl)methanol
α-D-glucopyranosyl-(1→4)-α-D-glucopyranosyl-(1→4)-α-D-sorbitol
Benzene, [4-(1-methylethyl)-3-cyclohexen-1-yl]-
pyridine-3-carbonitrile
4,4-Dimethyl-5-oxo-2-phenethyl-tetrahydro-furan-3-carboxylic acid ethyl ester
4-O-benzyl-1,2-O-(1-methoxyethylidene)-3-O-methyl-β-L-rhamnopyranose
3-(5-methyl-2-tetrahydrofuryl)-1-propanol
[(2R,4R,5S,6S,7R)-7,9-Bis-(tert-butyl-dimethyl-silanyloxy)-6-methoxy-2-methyl-5-trimethylsilanyloxy-4-(2-trimethylsilanyloxy-ethyl)-nonyloxymethyl]-benzene
