Journal article
3-HYDROXYMUSCARINES FROM L-RHAMNOSE
- Abstract:
- No protection is necessary for the synthesis of the muscarine analogue 3R-3-hydroxymuscarine from L-rhamnose; a sole silyl ether protecting group is required for the synthesis of 3S-3-hydroxymuscarine. Efficient construction of the tetrahydrofuran ring can be achieved either by ring contraction of the α-triflate of δ-rhamnonolactone, or by ring opening and closing of the α-triflate of γ-rhamnonolactone. © 1993.
- Publication status:
- Published
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- Publisher copy:
- 10.1016/S0040-4020(01)90162-0
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Authors
Bibliographic Details
- Journal:
- TETRAHEDRON
- Volume:
- 49
- Issue:
- 16
- Pages:
- 3343-3358
- Publication date:
- 1993-04-16
- DOI:
- ISSN:
-
0040-4020
- Source identifiers:
-
44100
Item Description
- Language:
- English
- Pubs id:
-
pubs:44100
- UUID:
-
uuid:c66d0c74-f3ed-41ec-b119-b41455d086fd
- Local pid:
- pubs:44100
- Deposit date:
- 2012-12-19
Terms of use
- Copyright date:
- 1993
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