Chemoenzymatic and enantioselective assembly of the (1α,3aβ,6α,7aβ)-octahydro-1,6-methano-1H-indene framework associated with 2-isocyanoallopupukeanane: validation of a new synthetic strategy and the identification of enantiomeric switching regimes-Reference-Cited by-同舟云学术

Chemoenzymatic and enantioselective assembly of the (1α,3aβ,6α,7aβ)-octahydro-1,6-methano-1H-indene framework associated with 2-isocyanoallopupukeanane: validation of a new synthetic strategy and the identification of enantiomeric switching regimes

Published:2010-07 Issue:27-28 Volume:66 Page:5250-5261
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Dietinger Christine E.,Banwell Martin G.,Garson Mary J.,Willis Anthony C.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference77 articles.

1. Two new sesquiterpene isonitriles from the nudibranch, phyllida pustulosa

2. 9-Isocyanopupukeanane, a marine invertebrate allomone with a new sesquiterpene skeleton

3. Defense Allomones of the NudibranchPhyllidia varicosa Lamarck 1801

4. Co-occurrence of 9-isocyanopupukeanane and its C-9 epimer in the nudibranch phyllidia bourguini

5. Isocyanoneopupukeanane, a new tricyclic sesquiterpene from a sponge

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