Multigram Synthesis of the C29−C51 Subunit and Completion of the Total Synthesis of Altohyrtin C (Spongistatin 2)-Reference-Cited by-同舟云学术

Multigram Synthesis of the C29−C51 Subunit and Completion of the Total Synthesis of Altohyrtin C (Spongistatin 2)

Published:2003-09-27 Issue:42 Volume:125 Page:12844-12849
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Heathcock Clayton H.¹,McLaughlin Mark¹,Medina Jesus¹,Hubbs Jed L.¹,Wallace Grier A.¹,Scott Robert¹,Claffey Michele M.¹,Hayes Christopher J.¹,Ott Gregory R.¹

Affiliation:

1. Contribution from the Center for New Directions in Organic Synthesis, Department of Chemistry, University of California, Berkeley, California 94720

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja030317%2B

Reference20 articles.

1. A Second-Generation Synthesis of the C1−C28 Portion of the Altohyrtins (Spongistatins)

2. Synthesis of the C29−C44 Portion of Spongistatin 1 (Altohyrtin A)

3. Readily accessible 12-I-5 oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones

4. A General Strategy for the Synthesis of Cladiellin Diterpenes: Enantioselective Total Syntheses of 6-Acetoxycladiell-7(16),11-dien-3-ol (Deacetoxyalcyonin Acetate), Cladiell-11-ene-3,6,7-triol, Sclerophytin A, and the Initially Purported Structure of Sclerophytin A

5. Organic synthesis using haloboration reaction. I. A simple and selective synthesis of 2-bromo- and 2-iodo-1-alkenes

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