A formal synthesis of 18-O-methyl mycalamide B

Synthesis

Volumn , Issue 12, 1999, Pages 2087-2095

  Kocienski, Philip J ^a   Raubo, Piotr ^a   Smith, Christopher ^a   Boyle, F Thomas ^b  

^a UNIVERSITY OF GLASGOW   (United Kingdom)

^b ASTRAZENECA   (United Kingdom)

Author keywords

1,3 dioxane synthesis; Addition reactions; Asymmetric dihydroxylation; Conjugate addition; Fleming Tamao oxidation; Grignard reaction; Osmium; Protecting groups; Reductions; Stereoselective hydroxylation of a ketone

Indexed keywords

18 O METHYLMYCALAMIDE B; ANTINEOPLASTIC AGENT; MYCALAMIDE B DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DRUG HYDROXYLATION; DRUG OXIDATION; DRUG STRUCTURE; DRUG SYNTHESIS; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 0032713609     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-1999-3633     Document Type: Article

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