Kim, Jiyool Kang, Jueun Han, Yongseong Sim, Jinchan Park, Young-Tae Kim, Young-Joo Kwon, Jaeyoung Cho, Ja Young Kim, Taejung 2026-01-13T07:30:30Z 2026-01-13T07:30:30Z 2026-01-12 2026-01 1477-0520 https://pubs.kist.re.kr/handle/201004/153992 This study demonstrates a concise four-step total synthesis of N-acyl-l-phenylalanine derivatives (P1-P5) from Micromonospora sp. MS-62 enabling definitive assignment of the S configuration at C-1 ' via single-crystal X-ray diffraction. This synthesis clarifies the stereochemistry of this natural product class and facilitates future exploration of structure-activity relationship. English Royal Society of Chemistry Synthesis-enabled conformational assignment of natural N-acyl l-phenylalanine derivatives from freshwater sponge–associated Micromonospora sp. MS-62 Article 10.1039/d5ob01886b 1 Organic & Biomolecular Chemistry, v.24, no.3, pp.597 - 600 Organic & Biomolecular Chemistry 24 3 597 600 N scie scopus 001652352600001 Chemistry, Organic Chemistry Article METHYL-ESTERS