REGIOSPECIFIC REDUCTIVE RING-CLEAVAGE OF N-SUBSTITUTED AZIRIDINE-2-CARBOXYLATES AND AN AZIRIDINE-2-METHANOL VIA CATALYTIC-HYDROGENATION USING PD AS A CATALYST

LIM, YH; LEE, WK

doi:10.1016/0040-4039(95)01814-X

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REGIOSPECIFIC REDUCTIVE RING-CLEAVAGE OF N-SUBSTITUTED AZIRIDINE-2-CARBOXYLATES AND AN AZIRIDINE-2-METHANOL VIA CATALYTIC-HYDROGENATION USING PD AS A CATALYST

LIM, YH;
LEE, WK

Citations

WEB OF SCIENCE

65

Citations

SCOPUS

70

초록

Regiospecific reductive ring cleavage was accomplished in the reaction of N-alpha-methylbenzyl substituted aziridine-2-carboxylate and aziridine-2-methanol under a catalytic hydrogenation condition, The regiospecificity was determined by the substituent at C-2.

키워드

AMINO-ACIDS; 2-AZIRIDINECARBOXYLIC ACID; ORGANOMETALLIC REAGENTS; OPENING REACTIONS; ESTERS; DERIVATIVES; AZIRIDINE

제목: REGIOSPECIFIC REDUCTIVE RING-CLEAVAGE OF N-SUBSTITUTED AZIRIDINE-2-CARBOXYLATES AND AN AZIRIDINE-2-METHANOL VIA CATALYTIC-HYDROGENATION USING PD AS A CATALYST

저자: LIM, YH; LEE, WK

DOI: 10.1016/0040-4039(95)01814-X

발행일: 1995-11-13

유형: Article

저널명: Tetrahedron Letters

권: 36

호: 46

페이지: 8431 ~ 8434