|
Volumn 49, Issue 2, 2013, Pages 193-195
|
A short and flexible route to tetrahydropyran-4-ones via conjugated nitrile oxides cycloaddition and oxa-Michael cyclization: A concise diastereoselective total synthesis of (±)-diospongin A
|
Author keywords
[No Author keywords available]
|
Indexed keywords
ALKENE DERIVATIVE;
DIOSPONGIN A;
NATURAL PRODUCT;
NITRILE OXIDE;
TETRAHYDROPYRAN DERIVATIVE;
UNCLASSIFIED DRUG;
ARTICLE;
CONJUGATION;
CYCLIZATION;
CYCLOADDITION;
DESILYLATION;
DIASTEREOISOMER;
MICHAEL ADDITION;
OXIDATION;
QUANTUM YIELD;
REACTION ANALYSIS;
REDUCTION;
RING OPENING;
STEREOCHEMISTRY;
|
EID: 84870564387
PISSN: 13597345
EISSN: 1364548X
Source Type: Journal
DOI: 10.1039/c2cc37772a Document Type: Article |
Times cited : (25)
|
References (17)
|