Concise synthesis of (+/-)-cytisine via lithiation of N-Boc-bispidine.

[reaction: see text] (+/-)-Cytisine has been synthesized in 19% overall yield via a six-step approach from commercially available materials. Key features of this new strategy are as follows: (i) initial construction of the bispidine core, (ii) lithiation-transmetalation-allylation of an N-Boc-bispidine, and (iii) a Pd/C-mediated dihydropyridone oxidation-N-debenzylation process.

[1]  Ningyi Chen,et al.  Regio- and enantioselective control in the reactions of alpha-(N-carbamoyl)alkylcuprates with allylic phosphates. , 2004, Organic letters.

[2]  F. Sparatore,et al.  Synthesis and preliminary pharmacological evaluation of some cytisine derivatives. , 1999, Farmaco.

[3]  D. Passarella,et al.  Total enantioselective synthesis of (-)-cytisine. , 2004, Organic letters.

[4]  J. Papillon,et al.  The preparation of nonracemic secondary alpha-(carbamoyloxy)alkylzinc and copper reagents. A versatile approach to enantioenriched alcohols. , 2002, Organic letters.

[5]  Chris M. Topping,et al.  Reactivity and enantioselectivity in the reactions of scalemic stereogenic alpha-(N-carbamoyl)alkylcuprates. , 2004, The Journal of organic chemistry.

[6]  T. Honda,et al.  Syntheses of (+)-cytisine, (-)-kuraramine, (-)-isokuraramine, and (-)-jussiaeiine A. , 2005, The Journal of organic chemistry.

[7]  J. Bénavidès,et al.  Synthesis of a [2-pyridinyl-18F]-labelled fluoro derivative of (-)-cytisine as a candidate radioligand for brain nicotinic alpha4beta2 receptor imaging with PET. , 2003, Bioorganic & medicinal chemistry.

[8]  A. Goldman,et al.  Efficient low-temperature thermal functionalization of alkanes. Transfer-dehydrogenation catalyzed by Rh(PMe3)2Cl(CO) in solution under a high pressure dihydrogen atmosphere , 1991 .

[9]  S. Arneric,et al.  Nicotinic receptor binding of [3H]cytisine, [3H]nicotine and [3H]methylcarbamylcholine in rat brain. , 1994, European journal of pharmacology.

[10]  W. Bailey,et al.  An experimental and computational investigation of the enantioselective deprotonation of Boc-piperidine. , 2002, Journal of the American Chemical Society.

[11]  E. E. Tamelen,et al.  Total Synthesis of Oxygenated Lupin Alkaloids1 , 1958 .

[12]  R. C. Crittendon,et al.  Transformations of Cyclohexane Derivatives in Supercritical Water , 1994 .

[13]  D. Yohannes,et al.  Total synthesis of (+/-)-cytisine. , 2000, Organic letters.

[14]  W. Weise,et al.  Zur Synthese des Cytisins, III. Mitteil.: Totalsynthese des Cytisins , 1956 .

[15]  P. Beak,et al.  .alpha.-Lithioamine synthetic equivalents: syntheses of diastereoisomers from Boc derivatives of cyclic amines , 1993 .

[16]  B. Thyagarajan,et al.  763. Synthesis of (±)-cytisine , 1957 .

[17]  P. Beak,et al.  α-Lithioamine synthetic equivalents from dipole-stabilized carbanions: the t-Boc group as an activator for α'-lithiation of carbamates , 1989 .

[18]  Sukbok Chang,et al.  A short and concise synthetic route to (−)-coniceine , 2001 .

[19]  E. E. Tamelen,et al.  THE SYNTHESIS OF dl-CYTISINE , 1955 .

[20]  V. Boido,et al.  Cytisine derivatives as ligands for neuronal nicotine receptors and with various pharmacological activities. , 2003, Farmaco.

[21]  F. Felpin,et al.  Recent Advances in the Total Synthesis of Piperidine and Pyrrolidine Natural Alkaloids with Ring‐Closing Metathesis as a Key Step , 2003 .

[22]  Alexander Deiters,et al.  Synthesis of oxygen- and nitrogen-containing heterocycles by ring-closing metathesis. , 2004, Chemical reviews.

[23]  Brian T. O’Neill,et al.  Varenicline: An α4β2 Nicotinic Receptor Partial Agonist for Smoking Cessation , 2005 .

[24]  Yasukazu Saito,et al.  Dehydrogeno-aromatization of cyclohexanes with suspended noble metal catalysts , 1991 .

[25]  P. O’Brien,et al.  Diastereoselective synthesis of sparteine analogues via lithiation–electrophilic quench of N-Boc bispidines , 2000 .

[26]  M. Kozlowski,et al.  Is the A-ring of sparteine essential for high enantioselectivity in the asymmetric lithiation-substitution of N-Boc-pyrrolidine? , 2004, Journal of the American Chemical Society.

[27]  J. Rouden,et al.  Synthesis of analogues of (-)-cytisine for in vivo studies of nicotinic receptors using positron emission tomography. , 2000, Organic letters.

[28]  V. Singh,et al.  Total synthesis of (-)- and (+)-lentiginosine. , 2002, The Journal of organic chemistry.

[29]  O. Nicolotti,et al.  Cytisine derivatives as high affinity nAChR ligands: synthesis and comparative molecular field analysis. , 2002, Farmaco.

[30]  J. Coe Total synthesis of (+/-)-cytisine via the intramolecular heck cyclization of activated N-alkyl glutarimides. , 2000, Organic letters.

[31]  M. Carda,et al.  Synthesis of conjugated δ-lactams using ring-closing metathesis , 2002 .

[32]  D. Passarella,et al.  New solution free and polymer anchored chiral bispidine-based amino alcohols. Synthesis and screening for the enantioselective addition of diethylzinc to benzaldehyde , 2003 .

[33]  T. Gallagher,et al.  A short synthesis of (+/-)-cytisine. , 2004, Organic and biomolecular chemistry.

[34]  S. Heinemann,et al.  Partial agonist properties of cytisine on neuronal nicotinic receptors containing the beta 2 subunit. , 1994, Molecular pharmacology.