An Efficient Synthesis of Valienamine via Ring-Closing Metathesis-Reference-Cited by-同舟云学术

An Efficient Synthesis of Valienamine via Ring-Closing Metathesis

Published:2005-03-17 Issue:8 Volume:70 Page:3299-3302
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Chang Young-Kil¹,Lee Bo-Young¹,Kim Dong Jun¹,Lee Gwan Sun¹,Jeon Heung Bae¹,Kim Kwan Soo¹

Affiliation:

1. Center for Bioactive Molecular Hybrids and Department of Chemistry, Yonsei University, Seoul 120-749, Korea, and Hanmi Research Center, Hanmi Pharmaceutical Co. Ltd., Gyeonggi-do 445-813, Korea kwan@yonsei.ac.kr; hbj@yonsei.ac.kr

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo047735x

Reference34 articles.

1. N-substituted valienamines, .ALPHA.-glucosidase inhibitors.

2. The unsaturated cyclitol part of the new antibiotics, the validamycins

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4. New intermediates, degradation of validamycin A by Flavobacterium saccharophilum.

5. Microbial degradation of validamycin A by Flavobacterium saccharophilum. Enzymatic cleavage of C-N linkage in validoxylamine A.

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