A Short Stereoselective Synthesis of Prepiscibactin Using a SmI2-Mediated Reformatsky Reaction and Zn2+-Induced Asymmetric Thiazolidine Formation

Yuri Segade; Marcos A. Montaos; Jaime Rodríguez; Carlos Jiménez

doi:10.1021/ol502958u

A Short Stereoselective Synthesis of Prepiscibactin Using a SmI2-Mediated Reformatsky Reaction and Zn2+-Induced Asymmetric Thiazolidine Formation

Organic Letters ◽

10.1021/ol502958u ◽

2014 ◽

Vol 16 (21) ◽

pp. 5820-5823 ◽

Cited By ~ 13

Author(s):

Yuri Segade ◽

Marcos A. Montaos ◽

Jaime Rodríguez ◽

Carlos Jiménez

Keyword(s):

Stereoselective Synthesis ◽

Reformatsky Reaction

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Chemoselective and stereoselective synthesis of gem-difluoro-β-aminoesters or gem-difluoro-β-lactams from ethylbromodifluoroacetate and imines during Reformatsky reaction

Tetrahedron ◽

10.1016/j.tet.2007.09.058 ◽

2007 ◽

Vol 63 (50) ◽

pp. 12352-12366 ◽

Cited By ~ 29

Author(s):

Nicolas Boyer ◽

Philippe Gloanec ◽

Guillaume De Nanteuil ◽

Philippe Jubault ◽

Jean-Charles Quirion

Keyword(s):

Stereoselective Synthesis ◽

Reformatsky Reaction

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ChemInform Abstract: A Highly Stereoselective Synthesis of a Key Intermediate (III) of 1β-Methylcarbapenems Employing the Reformatsky Reaction of 3-(2-Bromopropionyl)-2-oxazolidone Derivatives (II).

ChemInform ◽

10.1002/chin.198822192 ◽

1988 ◽

Vol 19 (22) ◽

Author(s):

Y. ITO ◽

S. TERASHIMA

Keyword(s):

Stereoselective Synthesis ◽

Reformatsky Reaction ◽

The Reformatsky Reaction

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A highly stereoselective synthesis of aldols employing the Reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives with various aldehydes

Tetrahedron Letters ◽

10.1016/s0040-4039(00)96931-4 ◽

1987 ◽

Vol 28 (52) ◽

pp. 6629-6632 ◽

Cited By ~ 11

Author(s):

Yoshio Ito ◽

Shiro Terashima

Keyword(s):

Stereoselective Synthesis ◽

Reformatsky Reaction ◽

The Reformatsky Reaction

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ChemInform Abstract: A Highly Stereoselective Synthesis of Aldols Employing the Reformatsky Reaction of 3-(2-Bromopropionyl)-2-oxazolidone Derivatives (I) with Various Aldehydes (II).

ChemInform ◽

10.1002/chin.198822191 ◽

1988 ◽

Vol 19 (22) ◽

Author(s):

Y. ITO ◽

S. TERASHIMA

Keyword(s):

Stereoselective Synthesis ◽

Reformatsky Reaction ◽

The Reformatsky Reaction

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A highly stereoselective synthesis of a key intermediate of 1β-methylcarbapenems employing the reformatsky reaction of 3-(2-bromopropionyl)-2-oxazolidone derivatives

Tetrahedron Letters ◽

10.1016/s0040-4039(00)96930-2 ◽

1987 ◽

Vol 28 (52) ◽

pp. 6625-6628 ◽

Cited By ~ 30

Author(s):

Yoshio Ito ◽

Shiro Terashima

Keyword(s):

Stereoselective Synthesis ◽

Reformatsky Reaction ◽

The Reformatsky Reaction

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Asymmetric zinc-Reformatsky reaction of Evans chiral imide with acetophenones and its application to the stereoselective synthesis of triazole antifungal agents

Tetrahedron Asymmetry ◽

10.1016/j.tetasy.2007.03.015 ◽

2007 ◽

Vol 18 (8) ◽

pp. 949-962 ◽

Cited By ~ 31

Author(s):

Luo-Ting Yu ◽

Meng-Tsung Ho ◽

Ching-Yao Chang ◽

Teng-Kuei Yang

Keyword(s):

Antifungal Agents ◽

Stereoselective Synthesis ◽

Reformatsky Reaction

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Stereoselective Synthesis (Part K)

10.1016/s1572-5995(06)x8144-9 ◽

1995 ◽

Keyword(s):

Stereoselective Synthesis

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Catalytic Stereoselective Synthesis of α-Amino Phosphonic Acid Derivatives by Asymmetric Hydrogenation

Synthetic Communications ◽

10.1080/00397919608003678 ◽

1996 ◽

Vol 24 (4) ◽

pp. 777-781 ◽

Cited By ~ 4

Author(s):

Ute Schmidt ◽

Günther Oehme ◽

Hanswalter Krause

Keyword(s):

Phosphonic Acid ◽

Stereoselective Synthesis ◽

Asymmetric Hydrogenation

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Stereoselective Synthesis By Robert S. Atkinson, University of Leicester. John Wiley & Sons, Inc., New York, NY. 1995. xii + 529 pp. 15 × 23 cm. $59.95. ISBN 0-471-954195.

Journal of Natural Products ◽

10.1021/np960463b ◽

1996 ◽

Vol 59 (12) ◽

pp. 1215-1216

Author(s):

Huw M. L. Davies

Keyword(s):

New York ◽

Stereoselective Synthesis

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Stereoselective Synthesis of 2-Deoxy-β-glycosides From Glycal Precursors. 1. Stereochemistry of the Reactions of ?-Glucal Derivatives with Phenylsulfenyl Chloride and Phenylselenenyl Chloride

Tetrahedron ◽

10.1016/s0040-4020(97)00571-1 ◽

1997 ◽

Vol 53 (26) ◽

pp. 8825-8836

Author(s):

W Roush*

Keyword(s):

Stereoselective Synthesis

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