Skip NavigationSkip to Content
Return Return to Search Results

Enantioselective synthesis of metathesis-derived ureapeptoid macrocycles

  1. Author:
    Wang, X. Z.
    Burke, T. R.

  2. Author Address

    Burke, TR, NCI, Med Chem Lab, Ctr Canc Res, NIH, Frederick, MD 21701 USA NCI, Med Chem Lab, Ctr Canc Res, NIH, Frederick, MD 21701 USA.
    1. Year: 2004
  2. Journal: Synlett
    1. 3
    2. Pages: 469-472
  4. Type of Article: Article
  1. Abstract:

    Ring-closing metathesis (RCM) was used for the preparation of the first member of a new class of ureapeptoid-containing macrocycles. Key to the approach was the enantioselective synthesis of functionalized carbamoyl alkenylglycine equivalents using (-)-B-allyldiisopinocampheylborane [(-)-d-Ipc(2)Ball]-mediated asymmetric allylation

    See More

  1. Keywords:

External Sources

  1. No sources found.

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel