An Asymmetric Synthesis of Aza Analogues of the Tricyclic Skeleton of Daphnane and the ABC Ring System of Phorbol-Reference-Cited by-同舟云学术

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An Asymmetric Synthesis of Aza Analogues of the Tricyclic Skeleton of Daphnane and the ABC Ring System of Phorbol

Published:2002-12-12 Issue:3 Volume:68 Page:792-798
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Marson Charles M.¹,Pink Jennifer H.¹,Hall David¹,Hursthouse Michael B.²,Malik Abdul³,Smith Christopher⁴

Affiliation:

1. Department of Chemistry, University of Sheffield, Sheffield, S3 7HF, U.K.

2. Department of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, U.K.

3. Department of Chemistry, University of Wales, P.O. Box 912, Park Place, Cardiff CF1 3TB, U.K.

4. Rhône-Poulenc Rorer Ltd., Rainham Road South, Dagenham, Essex RM10 7XS, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0205816

Reference38 articles.

1. Convergent, stereocontrolled routes to hydroxylated tricyclic systems: a new annulation of 2-cyclohexen-1-one

2. Lewis acid mediated reactions of 2,3-epoxyalcohols: an efficient stereocontrolled route to polycyclic diols

3. Computer-assisted molecular modeling of tumor promoters: rationale for the activity of phorbol esters, teleocidin B, and aplysiatoxin.

4. Analysis of the phorbol ester pharmacophore on protein kinase C as a guide to the rational design of new classes of analogs.

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2. Synthesis of Complex Stereoheptads en Route to Daphnane Diterpene Orthoesters;Organic Letters;2018-08-17

3. An Efficient Synthesis of Dihydrobenzo[c]azepines from Morita-Baylis-Hillman Adducts via Pictet-Spengler Reaction;Bulletin of the Korean Chemical Society;2016-04-06

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