Remote Stereocontrol in [3,3]-Sigmatropic Rearrangements: Application to the Total Synthesis of the Immunosuppressant Mycestericin G-Reference-Cited by-同舟云学术

Remote Stereocontrol in [3,3]-Sigmatropic Rearrangements: Application to the Total Synthesis of the Immunosuppressant Mycestericin G

Published:2012-01-12 Issue:3 Volume:14 Page:756-759
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Fairhurst Nathan W. G.¹,Mahon Mary F.¹,Munday Rachel H.¹,Carbery David R.¹

Affiliation:

1. Department of Chemistry, University of Bath, Bath, BA2 7AY, United Kingdom, and AstraZeneca R&D, Charnwood, Bakewell Road, Loughborough LE11 5RH, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol203300k

Reference63 articles.

1. Crystal and Molecular Structure of an Iodo-derivative of the Cyclic Undecapeptide Cyclosporin A

2. CYCLOSPORIN A IN PATIENTS RECEIVING RENAL ALLOGRAFTS FROM CADAVER DONORS

3. CYCLOSPORIN A FOR THE TREATMENT OF GRAFT-VERSUS-HOST DISEASE IN MAN

4. Natural products as immunosuppressive agents

5. MYRIOCIN, A NEW ANTIFUNGAL ANTIBIOTIC FROM MYRIOCOCCUM ALBOMYCES

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