Tetrahedron Letters p. 2381 - 2384 (1996)
Update date:2022-08-05
Topics:
Hoffman, Robert V.
Patonay, Tamas
Nayyar, Naresh K.
Tao, Junhua
Described herein is a four-step enantiospecific synthesis of a protected seco acid precursor of (R,R)-(-)-pyrenophorin in 23% yield from a chiral β-ketoester 3, which can be prepared in one step from ethyl acetoacetate by a standard procedure.
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Doi:10.1021/om9509608
(1996)Doi:10.1016/0040-4039(96)00303-6
(1996)Doi:10.1039/cc9960000813
(1996)Doi:10.1021/ja960126p
(1996)Doi:10.1016/S0040-4020(02)00369-1
(2002)Doi:10.1016/S0040-4020(01)81552-0
(1993)
