A new synthetic strategy for the penems. Total synthesis of (5R, 6S, 8R)-6-(. alpha.-hydroxyethyl)-2-(hydroxymethyl) penem-3-carboxylic acid

S Hanessian, A Bedeschi, C Battistini…

Index: Journal of the American Chemical Society, , vol. 107, # 5 p. 1438 - 1439

Full Text: HTML

Citation Number: 64

Abstract

... Chem. SOC. 1980,102, 2039-2043. (3) Ernest, I. In "Chemistry and Biology of the p-Lactam Antibiotics"; Morin, RB, Gorman, M., Eds.; Academic Press: New York, 1982; p 315. ... 2765-2768. 0 1985 American Chemical Society Page 2. J. Am. ... SOC. 1985, 107, 1439-1440 1439 \ ...

Related Articles:

Fe 2 O 3-catalyzed Baeyer-Villiger oxidation of ketones with molecular oxygen in the presence of aldehydes

[Murahashi, Shun-Ichi; Oda, Yoshiaki; Naota, Takeshi Tetrahedron Letters, 1992 , vol. 33, # 49 p. 7557 - 7560]

Scope and Limitations of Oxidative Decarboxylation of α-(Acylamino) Acids by Peroxy Acids: Conversion of a 2-Azetidinone-4-carboxylic Acid to a Carbapenem

[Shiozaki Synthesis, 1990 , # 8 p. 691 - 693]

Scope and Limitations of Oxidative Decarboxylation of α-(Acylamino) Acids by Peroxy Acids: Conversion of a 2-Azetidinone-4-carboxylic Acid to a Carbapenem

[Synthesis, , # 8 p. 691 - 693]

Scope and Limitations of Oxidative Decarboxylation of α-(Acylamino) Acids by Peroxy Acids: Conversion of a 2-Azetidinone-4-carboxylic Acid to a Carbapenem

[Synthesis, , # 8 p. 691 - 693]

More Articles...