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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 27, 1997 - Issue 11
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Original Articles

Synthesis of Chloramphenicol via a new Intermediate 4-para-Nitrophenyl-5-formamido-1,3-dioxane

Braja G Hazra Division of Organic Chemistry (Synthesis), National Chemical Laboratory, Pune, 411008, India
,
Vandana S. Pore Division of Organic Chemistry (Synthesis), National Chemical Laboratory, Pune, 411008, India
&
Shailaja P. Maybhate Division of Organic Chemistry (Synthesis), National Chemical Laboratory, Pune, 411008, India
Pages 1857-1864 | Received 13 Nov 1996, Published online: 22 Aug 2006

Citations (7)

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Read on this site (1)

B.G. Hazra, V.S. Pore, S.P. Maybhate, B.V. Bapat, V.K. Gumaste & A.S. Rao. (1999) NITRATION STUDIES ON 4-PHENYL-5-SUBSTIUTED-1,3-DIOXANES AS CHLORAMPHENICOL INTERMEDIATES. Organic Preparations and Procedures International 31:3, pages 315-319.
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Articles from other publishers (6)

Allegra Franchino, Pavol Jakubec & Darren J. Dixon. (2016) Enantioselective synthesis of (−)-chloramphenicol via silver-catalysed asymmetric isocyanoacetate aldol reaction. Organic & Biomolecular Chemistry 14:1, pages 93-96.
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Shyla George, Srinivasarao V. Narina & Arumugam Sudalai. (2006) A short enantioselective synthesis of (−)-chloramphenicol and (+)-thiamphenicol using tethered aminohydroxylation. Tetrahedron 62:43, pages 10202-10207.
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Saumen Hajra, Ananta Karmakar, Tapan Maji & Amiya Kumar Medda. (2006) Stereoselective syntheses of (−)-chloramphenicol and (+)-thiamphenicol. Tetrahedron 62:38, pages 8959-8965.
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G. Bhaskar, V. Satish Kumar & B. Venkateswara Rao. (2004) A short stereoselective synthesis of (−)-chloramphenicol and (+)-thiamphenicol. Tetrahedron: Asymmetry 15:8, pages 1279-1283.
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E.J. Corey & Soongyu Choi. (2000) Efficient enantioselective syntheses of chloramphenicol and (d)-threo- and (d)-erythro-sphingosine. Tetrahedron Letters 41:16, pages 2765-2768.
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B. G. HAZRA, V. S. PORE & S. P. MAYBHATE. (2010) ChemInform Abstract: Synthesis of Chloramphenicol via a New Intermediate 4‐para‐Nitrophenyl‐ 5‐formamido‐1,3‐dioxane.. ChemInform 28:35.
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