Synthesis of ring A of ambruticin and proof of its absolute stereochemistry
1980 ◽
Vol 58
(20)
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pp. 2173-2177
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Appropriately derivatized ambruticin was converted by reductive ozonolysis to tetrahydropyran 9c and cyclopropane 12a, which were synthesized from L-arabinose and (R)-Feist's acid in an unambiguous manner.
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2013 ◽
Vol 15
(5)
◽
pp. 566-573
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1984 ◽
Vol 25
(13)
◽
pp. 1371-1372
◽
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1994 ◽
Vol 116
(26)
◽
pp. 12097-12098
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1998 ◽
Vol 39
(5-6)
◽
pp. 463-466
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