- Home
- Publications
- Publication Search
- Publication Details
Title
Asymmetric Total Synthesis of Taxol
Authors
Keywords
-
Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 143, Issue 42, Pages 17862-17870
Publisher
American Chemical Society (ACS)
Online
2021-10-14
DOI
10.1021/jacs.1c09637
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Taxanes in cancer treatment: Activity, chemoresistance and its overcoming
- (2021) Luciana Mosca et al. DRUG RESISTANCE UPDATES
- Therapeutic strategies to overcome taxane resistance in cancer
- (2021) Tuyelee Das et al. DRUG RESISTANCE UPDATES
- Total Synthesis of Natural Products with Bridged Bicyclo[m.n.1] Ring Systems via Type II [5 + 2] Cycloaddition
- (2020) Long Min et al. ACCOUNTS OF CHEMICAL RESEARCH
- Total synthesis of the complex taxane diterpene canataxpropellane
- (2020) Fabian Schneider et al. SCIENCE
- Total Synthesis of Natural Products Containing a Bridgehead Double Bond
- (2020) Junyang Liu et al. Chem
- Recent Advances in the Total Synthesis of Natural Products Containing Eight-Membered Carbocycles (2009–2019)
- (2020) Ya-Jian Hu et al. CHEMICAL REVIEWS
- Two-Phase Synthesis of Taxol
- (2020) Yuzuru Kanda et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Two-Phase Total Synthesis of Taxanes: Tactics and Strategies
- (2020) Yuzuru Kanda et al. JOURNAL OF ORGANIC CHEMISTRY
- Total Synthesis of 1-Hydroxytaxinine
- (2019) Yusuke Imamura et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Asymmetric Total Synthesis of (−)-Vinigrol
- (2019) Long Min et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Total Synthesis of (+)-Pleuromutilin
- (2018) Elliot P. Farney et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Synthetic Study toward the Total Synthesis of Taxezopidines A and B
- (2018) Ya-Jian Hu et al. ORGANIC LETTERS
- Acyclic 1,4-Stereocontrol via the Allylic Diazene Rearrangement: Development, Applications, and the Essential Role of Kinetic E Stereoselectivity in Tosylhydrazone Formation
- (2017) Maha L. Shrestha et al. JOURNAL OF ORGANIC CHEMISTRY
- Short, Enantioselective Total Synthesis of Highly Oxidized Taxanes
- (2016) Changxia Yuan et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Accessing low-oxidation state taxanes: is taxadiene-4(5)-epoxide on the taxol biosynthetic pathway?
- (2016) Naomi A. Barton et al. Chemical Science
- Mechanistic Insights into Taxadiene Epoxidation by Taxadiene-5α-Hydroxylase
- (2015) Steven Edgar et al. ACS Chemical Biology
- Convergent Strategies in Total Syntheses of Complex Terpenoids
- (2015) Daisuke Urabe et al. CHEMICAL REVIEWS
- Synthesis of Paclitaxel. 2. Construction of the ABCD Ring and Formal Synthesis
- (2015) Keisuke Fukaya et al. ORGANIC LETTERS
- Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization
- (2015) Keisuke Fukaya et al. ORGANIC LETTERS
- Synthetic approaches and total syntheses of vinigrol, a unique diterpenoid
- (2015) Cristian Draghici et al. TETRAHEDRON
- Natural Products with Anti-Bredt and Bridgehead Double Bonds
- (2014) Jeffrey Y. W. Mak et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
- Cross-Coupling Reactions Using Samarium(II) Iodide
- (2014) Michal Szostak et al. CHEMICAL REVIEWS
- Formal Total Synthesis of (−)-Taxol through Pd-Catalyzed Eight-Membered Carbocyclic Ring Formation
- (2014) Sho Hirai et al. CHEMISTRY-A EUROPEAN JOURNAL
- Two-Phase Synthesis of (−)-Taxuyunnanine D
- (2014) Nathan C. Wilde et al. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
- Natural Taxanes: Developments Since 1828
- (2011) Yu-Fang Wang et al. CHEMICAL REVIEWS
- Scalable enantioselective total synthesis of taxanes
- (2011) Abraham Mendoza et al. Nature Chemistry
- Samarium Diiodide Mediated Reactions in Total Synthesis
- (2009) K. C. Nicolaou et al. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started