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Journal of Organic Chemistry

Volumn 67, Issue 12, 2002, Pages 4200-4208

Novel approach to the Zaragozic acids. Enantioselective total synthesis of 6,7-dideoxysqualestatin H5

(5) Naito, Satoru a Escobar, Maya a Kym, Philip R a Liras, Spiros a Martin, Stephen F a

a UNIVERSITY OF TEXAS AT AUSTIN (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL STEPS;

OXIDATION; SAPONIFICATION; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

ORGANIC ACIDS;

6,7 DIDEOXYSQUALESTATIN H5; ACETAL; ACID; ALCOHOL; BISLACTONE; ERYTHRONOLACTONE; ESTER DERIVATIVE; ETHER DERIVATIVE; FUROIC ESTER; LACTONE DERIVATIVE; SQUALESTATIN; TRIMETHYLSILYL ETHER DERIVATIVE; UNCLASSIFIED DRUG; ZARAGOSIC ACID DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; OXIDATION; SAPONIFICATION; STEREOCHEMISTRY; SYNTHESIS;

ACETALS; BICYCLO COMPOUNDS, HETEROCYCLIC; CATALYSIS; CHEMISTRY, ORGANIC; CYCLIZATION; KETONES; LACTONES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; STEREOISOMERISM; TRICARBOXYLIC ACIDS;

EID: 0037076999 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo011157s Document Type: Article

Times cited : (38)

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