Paclitaxel total synthesis

Molecular structure of paclitaxel.
Crystal structure of paclitaxel.

Paclitaxel total synthesis in organic chemistry is a major ongoing research effort in the total synthesis of paclitaxel (Taxol).[1] This diterpenoid is an important drug in the treatment of cancer but, also expensive because the compound is harvested from a scarce resource, namely the Pacific yew (Taxus brevifolia). Not only is the synthetic reproduction of the compound itself of great commercial and scientific importance, but it also opens the way to paclitaxel derivatives not found in nature but with greater potential.

The paclitaxel molecule consists of a tetracyclic core called baccatin III and an amide tail. The core rings are conveniently called (from left to right) ring A (a cyclohexene), ring B (a cyclooctane), ring C (a cyclohexane) and ring D (an oxetane).

The paclitaxel drug development process took over 40 years. The anti-tumor activity of a bark extract of the Pacific yew tree was discovered in 1963 as a follow up of a US government plant screening program already in existence 20 years before that. The active substance responsible for the anti-tumor activity was discovered in 1969 and structure elucidation was completed in 1971. Robert A. Holton of Florida State University succeeded in the total synthesis of paclitaxel in 1994, a project that he had started in 1982. In 1989 Holton had also developed a semisynthetic route to paclitaxel starting from 10-deacetylbaccatin III. This compound is a biosynthetic precursor and is found in larger quantities than paclitaxel itself in Taxus baccata (the European Yew). In 1990 Bristol-Myers Squibb bought a licence to the patent for this process which in the years to follow earned Florida State University and Holton (with a 40% take) over 200 million US dollars.

Total synthesis

The total synthesis of taxol is called one of the most hotly contested of the 1990s [2] with around 30 competing research groups by 1992. The number of research groups actually having reported a total synthesis currently stands at 9 with the Holton group (article first accepted for publication) and the Nicolaou group (article first published) first and second in what is called a photo finish.

Some of the efforts are truly synthetic but in others a precursor molecule found in nature is included. The key data are collected below. What all strategies have in common is synthesis of the baccatin molecule followed by last stage addition of the tail, a process (except for one) based on the Ojima lactam.

  1. Holton Taxol total synthesis - year: 1994 - precursor: Patchoulol - strategy: linear synthesis AB then C then D - references: see related article
  2. Nicolaou Taxol total synthesis - year: 1994 - precursor: Mucic acid strategy: convergent synthesis A and C merge to ABC then D - references: see related article[3]
  3. Danishefsky Taxol total synthesis - year: 1996 - precursor: Wieland-Miescher ketone strategy: convergent synthesis C merges with D then with A merges to ABCD - references: See related article
  4. Wender Taxol total synthesis - year: 1997 - precursor: Pinene strategy: linear synthesis AB then C then D - references:[4][5]
  5. Kuwajima Taxol total synthesis I. Kuwajima, - year: 1998 - precursor: synthetic building blocks strategy: linear synthesis A then B then C then D [6][7]
  6. Mukaiyama Taxol total synthesis T. Mukaiyama, - year: 1998 [8] - Precursor: L-serine strategy: linear synthesis B, then C, then A then D. References: see related article.
  7. Takahashi Taxol total synthesis T. Takahashi, - year: 2006 [9] - Precursor: geraniol strategy: convergent synthesis A and C merge to ABC then D
  8. Sato-Chida Taxol total synthesis Reported in 2015, formal synthesis to a Takahashi intermediate [10] [11] [12]
  9. Nakada Taxol total synthesis Reported in 2015, formal synthesis to a Takahashi intermediate [13]

Ongoing research efforts are directed at the synthesis of taxadiene and taxadienone intermediates.

Semisynthesis

The commercial semisynthesis (by Bristol-Myers Squibb) of paclitaxel starting from 10-deacetylbaccatin III (isolated from the European yew) is based on tail addition of the so-called Ojima lactam to its free hydroxyl group:

Semisynthesis of taxol from 10-deacetylbaccatin and (3R,4S)-3-triethylsilanyloxy-4-phenyl-N-Boc-2-azetidinone

Another commercial semisynthesis (by the company Natural Pharmaceuticals) relies on the isolation of a group of paclitaxel derivatives isolated from primary ornamental taxanes. These derivatives have the same skeleton as paclitaxel except for the organic residue R of the terminal tail amide group which can be phenyl, or propyl or pentyl (among others) whereas in paclitaxel it is an explicit phenyl group. The semisynthesis consists of conversion of the amide group to an amine with Schwartz's reagent through an imine followed by acidic workup and a benzoylation.

In the production process Michigan grown yews which mature in 8 years are periodically topped and dried. This material is shipped to Mexico for a first extraction step (10% paclitaxel content) and then to Canada for further purification to 95% purity. The semisynthesis to final product takes place in China.[14]

Biosynthesis

The biosynthetic pathway to paclitaxel has been investigated and consists of approximately 20 enzymatic steps. The complete scheme is still unavailable. The segments that are known are very different from the synthetic pathways tried thus far (Scheme 1). The starting compound is geranylgeranyl diphosphate 2 [15] which is a dimer of geraniol 1. This compound already contains all the required 20 carbon atoms for the paclitaxel skeleton. More ring closing through intermediate 3 (taxadiene) leads to taxusin 4. The two main reasons why this type of synthesis is not feasible in the laboratory is that nature does a much better job controlling stereochemistry and a much better job activating a hydrocarbon skeleton with oxygen substituents for which cytochrome P450 is responsible in some of the oxygenations. Intermediate 5 is called 10-deacetylbaccatin III.

A biochemical kilogram-scale production of taxadiene has been reported using genetically engineered E. coli.[16]

References and notes

  1. ↑ Note that the original publications about the total synthesis use the name "taxol", which used to be the generic name before it was accepted as a trademark in 1992.
  2. ↑ Creating complexity – the beauty and logic of synthesis Nina Hall Chem. Commun., 2003, 661 - 664, doi:10.1039/b212248k
  3. ↑ Nicolaou, K.C.; Z. Yang; J. J. Liu; H. Ueno; P. G. Nantermet; R. K. Guy; C. F. Claiborne; J. Renaud; E. A. Couladouros; K. Paulvannan; E. J. Sorenson (17 February 1994). "Total synthesis of taxol". Nature 367 (6464): 630–634. Bibcode:1994Natur.367..630N. doi:10.1038/367630a0. PMID 7906395.
  4. ↑ The Pinene Path to Taxanes. 5. Stereocontrolled Synthesis of a Versatile Taxane Precursor Paul A. Wender et al.J. Am. Chem. Soc.; 1997; 119(11) pp 2755 - 2756; (Communication) doi:10.1021/ja9635387
  5. ↑ The Pinene Path to Taxanes. 6. A Concise Stereocontrolled Synthesis of Taxol Wender, P. A. et al. J. Am. Chem. Soc.; (Communication); 1997; 119(11); 2757-2758. doi:10.1021/ja963539z
  6. ↑ Enantioselective Total Synthesis of Taxol Koichiro Morihira, Ryoma Hara, Shigeru Kawahara, Toshiyuki Nishimori, Nobuhito Nakamura, Hiroyuki Kusama, and Isao Kuwajima J. Am. Chem. Soc.; (Communication); 1998; 120(49); 12980-12981. DOI 10.1021/ja9824932
  7. ↑ Enantioselective Total Synthesis of (−)-Taxol Hiroyuki Kusama, Ryoma Hara, Shigeru Kawahara, Toshiyuki Nishimori, Hajime Kashima, Nobuhito Nakamura, Koichiro Morihira, and Isao Kuwajima. J. Am. Chem. Soc.; (Article); 2000; 122(16); 3811-3820. doi:10.1021/ja9939439
  8. ↑ New Method for the Synthesis of Baccatin III Isamu Shiina, Hayato Iwadare, Hiroki Sakoh, Masatoshi Hasegawa, Yu-ichirou Tani, and Teruaki Mukaiyama 1-2 1998 Chemistry Letters
  9. ↑ A Formal Total Synthesis of Taxol Aided by an Automated Synthesizer Takayuki Doi, Shinichiro Fuse, Shigeru Miyamoto, Kazuoki Nakai, Daisuke Sasuga and Takashi Takahashi Chemistry an Asian J.; (Article); 2006; 1(3); 370-383. DOI Abstract
  10. ↑ Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization Keisuke Fukaya, Yuta Tanaka, Ayako C. Sato, Keisuke Kodama, Hirohisa Yamazaki, Takeru Ishimoto, Yasuyoshi Nozaki, Yuki M. Iwaki, Yohei Yuki, Kentaro Umei, Tomoya Sugai, Yu Yamaguchi, Ami Watanabe, Takeshi Oishi, Takaaki Sato, and Noritaka Chida Organic Letters 2015 17 (11), 2570-2573 doi:10.1021/acs.orglett.5b01173
  11. ↑ Synthesis of Paclitaxel. 2. Construction of the ABCD Ring and Formal Synthesis Keisuke Fukaya, Keisuke Kodama, Yuta Tanaka, Hirohisa Yamazaki, Tomoya Sugai, Yu Yamaguchi, Ami Watanabe, Takeshi Oishi, Takaaki Sato, and Noritaka Chida Organic Letters 2015 17 (11), 2574-2577 doi:10.1021/acs.orglett.5b01174
  12. ↑ The Sato/Chida Synthesis of Paclitaxel D. F. Taber, Org. Chem. Highlights 2015, October 5. URL: http://www.organic-chemistry.org/Highlights/2015/05October.shtm
  13. ↑ Hirai, S., Utsugi, M., Iwamoto, M. and Nakada, M. (2015), Formal Total Synthesis of (−)-Taxol through Pd-Catalyzed Eight-Membered Carbocyclic Ring Formation. Chem. Eur. J., 21: 355–359. doi:10.1002/chem.201404295
  14. ↑ Paclitaxel from Primary Taxanes: A Perspective on Creative Invention in Organozirconium Chemistry Bruce Ganem and Roland R. Franke J. Org. Chem.; 2007; 72(11) pp 3981 - 3987; (Perspective) doi:10.1021/jo070129s
  15. ↑ Taxol Biosynthesis: Molecular Cloning and Characterization of a Cytochrome P450 Taxoid 7β-Hydroxylase MyDoanh Chau, Stefan Jennewein, Kevin Walker, and Rodney Croteau Chemistry and Biology, Vol 11, 663-672, May 2004 Abstract
  16. ↑ Ajikumar, P. K.; Xiao, W.-H.; Tyo, K. E. J.; Wang, Y.; Simeon, F.; Leonard, E.; Mucha, O.; Phon, T. H.; Pfeifer, B.; et al. (2010). "Isoprenoid Pathway Optimization for Taxol Precursor Overproduction in Escherichia coli". Science 330 (6000): 70–4. Bibcode:2010Sci...330...70A. doi:10.1126/science.1191652. PMC 3034138. PMID 20929806.

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