RCM is a powerful organic synthesis technique that involves the cleavage and formation of carbon-carbon double bonds within a molecule to create a cyclic structure. It is catalyzed by transition metal catalysts, such as ruthenium-based catalysts. RCM has gained popularity as a versatile tool for the construction of various cyclic and spirocyclic compounds.
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5-phenyl-2-[(5-phenyl-2H-tetrazol-2-yl)methyl]thieno[2,3-d]pyrimidin-4(3H)-one
(S)-methyl 2-(2,5-dihydro-1H-pyrrol-1-yl)-3-phenylpropanoate
C15H20O3
(4aR,6S,7S,8S,8aR)-6-allyl-8-(benzyloxy)-2,2-di-tert-butyl-7-methylhexahydropyrano[3,2-d][1,3,2]dioxasilin-7-ol
6-(4-Hydroxy-butyl)-2-phenyl-3,4-dihydro-2H-pyran-4-ol
toluene-4-sulfonic acid (2'R,3'S)-3'-but-3-enylxytetrahydropyran-2'-ylmethyl ester
2-[3-allyloxy-3-oxopropyl]phenyl 3-allyloxybenzoate
n
1,1'-bis(2-nitrophenylsulfonyl)-2,2',5,5'-tetrahydro-1H,1'H-3,3'-bipyrrole
C18H30O5Si2
<3R,4S,5S>-3-methoxy-5-<(p-methoxybenzyl)oxy>-6,6-dimethyl-4-(triethylsiloxy)-7-(trimethylsiloxy)-7-octenyl pivalate
C14H27NO2Si
1,2-O-Isopropylidene-4-O-(4-toluenesulfonyl)-D-threitol
[(2S,3R,4R,5S)-4-Benzyloxy-2-methoxy-5-(4-methoxy-benzyloxy)-6-methylene-tetrahydro-pyran-3-yl]-(4-methoxy-benzyl)-carbamic acid benzyl ester
(S)-(1S,3aS,6aS)-1-(1,3a,6,6a-Tetrahydro-pentalen-1-yl)-ethane-1,2-diol
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-4-fluoro-N-methyl-3-nitro-
(1R,2S)-1-phenyl-3-butene-1,2-diol
(+)-(S)-1-(phenylthio)pentan-2-ol
N-[4-chloro-3-(trifluoromethyl)phenyl]carbamoyl chloride
3-(allyl-benzyl-amino)-propionic acid methyl ester
cis-5-(methoxymethoxymethyl)cyclohex-2-enol
3-O-benzyl-5,6-dideoxy-1,2-O-isopropylidene-5-(N-benzyl-N-propenylamino)-α-D-gluco-7-eno-octo-1,4-furanose
N-(p-Nitrobenzyl)-2-methylen-4,4-dimethyl-pyrrolidin
