Applications of Zr-catalyzed carbomagnesation and Mo-catalyzed macrocyclic ring closing metathesis in asymmetric synthesis. Enantioselective synthesis of Sch 38516 (Fluvirucin B1)

K. A. Scheidt; W. R. Roush; A. F. Houri; D. S. La; D. A. Cogan; G. E. Hofilena; A. H. Hoveyda

Applications of Zr-catalyzed carbomagnesation and Mo-catalyzed macrocyclic ring closing metathesis in asymmetric synthesis. Enantioselective synthesis of Sch 38516 (Fluvirucin B₁)

K. A. Scheidt^*, W. R. Roush, A. F. Houri, D. S. La, D. A. Cogan, G. E. Hofilena, A. H. Hoveyda

^*Corresponding author for this work

Chemistry

Research output: Contribution to journal › Review article › peer-review

Abstract

For the synthesis of the antifungal agent Sch 38516. Hoveyda has employed a number of important transition metal-catalyzed reactions, including a ring-closing metathesis reaction to close the macrocycle present in this natural product.

Original language	English (US)
Pages (from-to)	522-530
Number of pages	9
Journal	Chemtracts
Volume	11
Issue number	7
State	Published - Jun 1 1998

ASJC Scopus subject areas

Chemistry(all)
Biochemistry
Molecular Biology

Cite this

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title = "Applications of Zr-catalyzed carbomagnesation and Mo-catalyzed macrocyclic ring closing metathesis in asymmetric synthesis. Enantioselective synthesis of Sch 38516 (Fluvirucin B1)",

abstract = "For the synthesis of the antifungal agent Sch 38516. Hoveyda has employed a number of important transition metal-catalyzed reactions, including a ring-closing metathesis reaction to close the macrocycle present in this natural product.",

author = "Scheidt, {K. A.} and Roush, {W. R.} and Houri, {A. F.} and La, {D. S.} and Cogan, {D. A.} and Hofilena, {G. E.} and Hoveyda, {A. H.}",

year = "1998",

month = jun,

day = "1",

language = "English (US)",

volume = "11",

pages = "522--530",

journal = "Chemtracts",

issn = "1431-9268",

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TY - JOUR

T1 - Applications of Zr-catalyzed carbomagnesation and Mo-catalyzed macrocyclic ring closing metathesis in asymmetric synthesis. Enantioselective synthesis of Sch 38516 (Fluvirucin B1)

AU - Scheidt, K. A.

AU - Roush, W. R.

AU - Houri, A. F.

AU - La, D. S.

AU - Cogan, D. A.

AU - Hofilena, G. E.

AU - Hoveyda, A. H.

PY - 1998/6/1

Y1 - 1998/6/1

N2 - For the synthesis of the antifungal agent Sch 38516. Hoveyda has employed a number of important transition metal-catalyzed reactions, including a ring-closing metathesis reaction to close the macrocycle present in this natural product.

AB - For the synthesis of the antifungal agent Sch 38516. Hoveyda has employed a number of important transition metal-catalyzed reactions, including a ring-closing metathesis reaction to close the macrocycle present in this natural product.

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UR - http://www.scopus.com/inward/citedby.url?scp=0031725717&partnerID=8YFLogxK

M3 - Review article

AN - SCOPUS:0031725717

VL - 11

SP - 522

EP - 530

JO - Chemtracts

JF - Chemtracts

SN - 1431-9268

IS - 7

ER -

Applications of Zr-catalyzed carbomagnesation and Mo-catalyzed macrocyclic ring closing metathesis in asymmetric synthesis. Enantioselective synthesis of Sch 38516 (Fluvirucin B₁)

Abstract

ASJC Scopus subject areas

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