Substituierte 9‐Oxabicyclo[4.2.1]‐ und 9‐Oxabicyclo[3.3.1]nonane IV .  endo, endo ‐2,5‐Dihydroxy‐9‐oxabicyclo[4.2.1]nonan,  endo, endo ‐,  endo, exo ‐ und  exo, exo ‐2,6‐Dihydroxy sowie  endo ,  exo ‐2,7‐Dihydroxy‐9‐oxabicyclo[3.3.1]nonan; Darstellung und Umwandlungsprodukte | Zendy

Duthaler R. O. | Zendy; Wicker K. | Zendy; Ackermann P. | Zendy; Ganter C. | Zendy

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Substituierte 9‐Oxabicyclo[4.2.1]‐ und 9‐Oxabicyclo[3.3.1]nonane IV . endo, endo ‐2,5‐Dihydroxy‐9‐oxabicyclo[4.2.1]nonan, endo, endo ‐, endo, exo ‐ und exo, exo ‐2,6‐Dihydroxy sowie endo , exo ‐2,7‐Dihydroxy‐9‐oxabicyclo[3.3.1]nonan; Darstellung und Umwandlungsprodukte

Author(s) -

Duthaler R. O.,

Wicker K.,

Ackermann P.,

Ganter C.

Publication year - 1972

Publication title -

helvetica chimica acta

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.74

H-Index - 82

eISSN - 1522-2675

pISSN - 0018-019X

DOI - 10.1002/hlca.19720550540

Subject(s) - nonane , chemistry , stereochemistry

The synthesis of the following compounds and reaction products thereof are described: endo , endo ‐2,5‐dihydroxy‐9‐oxabicyclo[4.2.1]nonane ( 3–5 ), epimeric 2,6‐dihydroxy‐9‐oxabicyclo[3.3.1]nonanes ( endo , endo : 6–8 , exo , exo : 29–32 , and endo , exo : 43–45 ), and endo , exo 2,7‐dihydroxy‐9‐oxabicyclo[3.3.1]nonane ( 46–50 ).

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