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- W1977568102 abstract "Ring closing metathesis of diallylglycine 6 provided cyclic Z-olefin 7 in 80% yield. The reaction was promoted by substitution of the amide nitrogen with the 2,4-dimethoxybenzyl group allowing for the required cis diallylglycine amide rotamer. Removal of the protecting groups provided cyclic dipeptide 2, a constrained scaffold useful in peptidomimetic research." @default.
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- W1977568102 date "2001-03-01" @default.
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- W1977568102 title "Synthesis of an Eight-Membered Cyclic Pseudo-Dipeptide Using Ring Closing Metathesis" @default.
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- W1977568102 doi "https://doi.org/10.1021/ol015530u" @default.
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