Cyclononitols: a flexible synthetic approach towards nine-membered carbasugar analogues

Tetrahedron Letters

Volumn 50, Issue 31, 2009, Pages 4519-4522

  Mehta, Goverdhan ^a,b   Pallavi, Kotapalli ^a   Katukojvala, Sreenivas ^b  

^a INDIAN INSTITUTE OF SCIENCE   (India)

^b INSTITUTE OF LIFE SCIENCES   (India)

Author keywords

[No Author keywords available]

Indexed keywords

CARBASUGAR; CARBONYL DERIVATIVE; CYCLONONITOL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; DEPROTECTION REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; HYDROXYLATION; STEREOCHEMISTRY;

EID: 66949179738     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.05.082     Document Type: Article

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26. 2 = 0.0905, G.O.F = 1.115 for all data, CCDC 629485.
27. We have also observed that other electrophilic additions to 23, such as epoxidation also proceed preferentially from the endo-face, thus further reinforcing our proposition.