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Volumn 79, Issue 11, 2001, Pages 1659-1667

Structure assignment of aminoconduritols by 15N NMR correlation spectroscopy; synthesis of a positional isomer of 7-deoxypancratistatin

(5) Schilling, Stefan a Rinner, Uwe a Chan, Collin a Ghiviriga, Ion a Hudlicky, Tomas a

a University of Florida ^* (United States)

Author keywords

15N NMR spectroscopy; Aminoconduritols; Iso 7 deoxypancratistatin; Lewis acid catalyzed intramolecuar opening of epoxides

Indexed keywords

NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS (CHEMICAL);

STRUCTURE ASSIGNMENTS;

ISOMERS;

2 ACETYLAMINO 1,3,4 TRIACETOXY 1,2,3,4,4A,11B HEXAHYDRO 1H 5,8,10 TRIOXACYCLOPENTA[B]PHENANTHRENE 6 ONE; 5,6 (ISOPROPYLIDENEDIOXY) 3 (4' METHYLPHENYLSULFONYL) 8 OXA 3 AZATRICYCLO[5.1.0.0]OCTANE; 7 DEOXYPANCREASTATIN; ACETIC ACID DERIVATIVE; AZIRIDINE DERIVATIVE; CONDURITOL AZIRIDINE; EPOXIDE; HEXANE; KETONE DERIVATIVE; OCTANE; PANCREASTATIN; UNCLASSIFIED DRUG; [2 (BENZO[1,3]DIOXOL 5 YLMETHOXY) 3 [N BENZYL(4' METHYLPHENYLSULFONYL)AMINO] 1,6 DIHYDROXY 4,5 (ISOPROPYLIDENEDIOXY)]HEXANE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; ISOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 0035684209 PISSN: 00084042 EISSN: None Source Type: Journal
DOI: 10.1139/v01-139 Document Type: Article

Times cited : (21)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.