An approach to the C(10)–C(16) fragment of the bryostatins: stereoselective exocyclic double-bond formation by vinyl radical cyclization-Reference-Cited by-同舟云学术

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An approach to the C(10)–C(16) fragment of the bryostatins: stereoselective exocyclic double-bond formation by vinyl radical cyclization

Published:1998 Issue:17 Volume: Page:2853-2864
ISSN:0300-922X
Container-title:Journal of the Chemical Society, Perkin Transactions 1
language:
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Maguire Robert J.,Munt Simon P.,Thomas Eric J.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1998/P1/A803422B

Cited by 38 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The evolution of a stereoselective synthesis of the C1–C16 fragment of bryostatins;Organic & Biomolecular Chemistry;2016

2. Preparation of conjugated dienoates with Bestmann ylide: Towards the synthesis of zampanolide and dactylolide using a facile linchpin approach;Beilstein Journal of Organic Chemistry;2015-10-05

3. Lyngbouilloside and Related Macrolides from Marine Cyanobacteria;Natural Product Communications;2013-07

4. Recent efforts to construct the B-ring of bryostatins;Chemical Communications;2013

5. Cascading Radical Cyclization of Bis-Vinyl Ethers: Mechanistic Investigation Reveals a 5-exo/3-exo/retro-3-exo/5-exo Pathway;The Journal of Organic Chemistry;2012-09-21

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