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Highly enantioenriched 2-azabenzonorbornenes from 7-azabenzonorbornadienes by asymmetric hydroboration-oxidation and tandem deoxygenation-rearrangement-electrophile trapping

Abstract:
3-exo-Substituted 2-azabenzonorbornenes are accessible from 7-azabenzonorbornadienes in good yields and high enantiomeric excess via asymmetric hydroboration-oxidation, followed by tandem deoxygenation- rearrangement-electrophile trapping and also provide access to substituted aminomethylindenes. © Georg Thieme Verlag Stuttgart.
Publication status:
Published

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Publisher copy:
10.1055/s-2006-950418

Authors


More by this author
Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Winning, LH More by this author
Journal:
SYNLETT
Volume:
2006
Issue:
15
Pages:
2476-2479
Publication date:
2006-09-18
DOI:
EISSN:
1437-2096
ISSN:
0936-5214
URN:
uuid:f0dda08e-fe7f-4a6b-b2b6-1fc63c38829a
Source identifiers:
40146
Local pid:
pubs:40146

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