1989
DOI: 10.1002/chin.198935217
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ChemInform Abstract: The Chemistry of Vicinal Tricarbonyl Compounds. Applications in the Synthesis of Isoquinoline Alkaloids.

Abstract: Coupling of the benzoyl chlorides (I) with the tert‐butoxycarbonylmethylenephosphorane (II), followed by ozonolysis, produces the α,β‐diketo esters (IV).

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1989
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“…When substituted on /Mactam rings, they have served as acceptor centers for the construction of the fused 4,5-bicyclic systems of carbapenams and penems.1 In combination with neighboring ester or vinyl groups, they have taken part in cyclization reactions leading to vincamine,2 erythrina,3 and phthalideisoquinoline alkaloids. 4 Other applications have been reported in the synthesis of hy-droxypyrroles5 including the bacterial pigment, prodigiosin.6…”
mentioning
confidence: 99%
“…When substituted on /Mactam rings, they have served as acceptor centers for the construction of the fused 4,5-bicyclic systems of carbapenams and penems.1 In combination with neighboring ester or vinyl groups, they have taken part in cyclization reactions leading to vincamine,2 erythrina,3 and phthalideisoquinoline alkaloids. 4 Other applications have been reported in the synthesis of hy-droxypyrroles5 including the bacterial pigment, prodigiosin.6…”
mentioning
confidence: 99%