Реакция #426497

ord-64daa086735f46e99aa6cad8e6fa2b2c

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Prepared in a similar manner to example 1 using benzo[d][1,3]dioxole-5-carbonyl chloride and D-leucine methyl ester hydrochloride. Yield: 83%. 1H NMR (500 MHz, CDCl3): δ 0.98 (m, 6H); 1.63-1.67 (m, 1H); 1.71-1.76 (m, 2H); 3.76 (s, 3H); 4.83 (m, 1H); 6.03 (s, 2H); 6.38 (d, 1H); 6.83 (d, 1H); 7.32 (s, 1H); 7.33 (d, 1H). MS (M+H, 294). m.p: 89-90° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08895050B2uspto-grants-2014_11