A racemic formal total synthesis of clavukerin A using gold(I)-catalyzed cycloisomerization of 3-methoxy-1,6-enynes as the key strategy

• Jae Youp Cheong and
• Young Ho Rhee

Beilstein J. Org. Chem. 2011, 7, 740–743, doi:10.3762/bjoc.7.84

• -catalyzed cycloisomerization of a 3-methoxy-1,6-enyne 5 as the key strategy followed by Rh-catalyzed stereoselective hydrogenation of the cycloheptenone 4. Keywords: clavukerin A; cycloisomerization; gold catalyst; hydrogenation; stereoselectivity; Findings Clavukerin A is a member of marine trinorguaiane

• followed by several other racemic and enantioselective syntheses [2][3][4][5][6][7][8][9][10][11][12][13][14]. Herein, we report a short formal total synthesis of racemic clavukerin A employing the gold(I)-catalyzed cycloisomerization of a 3-methoxy-1,6-enyne as the key strategy, which was recently

• cyclization (path B). The cycloheptenone 4 could then be synthesized from the enyne substrate 5 by gold(I)-catalyzed cycloisomerization. The synthesis of enyne substrate 5 commenced with the alkylation of methyl acetoacetate with the known bromide 6 [24] to provide compound 7 in 55% yield (Scheme 2

When cyclopropenes meet gold catalysts

• Frédéric Miege,
• Christophe Meyer and
• Janine Cossy

Beilstein J. Org. Chem. 2011, 7, 717–734, doi:10.3762/bjoc.7.82

• electron-deficient groups (Scheme 25) [24]. Besides these examples of intermolecular cyclopropanations, examples of intramolecular cyclopropanation of olefins by gold carbenes generated from cyclopropenes have been investigated in our group. Intramolecular cyclopropanation: cycloisomerization of

• , AuCl, [(Ph3P)AuNTf2], [(Ph3P)AuSbF6] or [(Ph3P)AuOTf]} were found to catalyze smoothly the cycloisomerization and yield the desired oxabicyclic compound 60 in high yields and with excellent diastereoselectivity (dr > 96:4) [25]. The observed stereochemical outcome has been tentatively rationalized by

• highlighted by the behaviour of geranyl ether 62d and neryl ether 62e, which furnished the epimeric cycloisomerization products 63d and 63e, respectively. The stereoselectivity was lower for methallyl ether 62f which afforded compound 63f as an 87:13 mixture of diastereomers (Scheme 27) [25]. The influence of

Gold-catalyzed heterocyclizations in alkynyl- and allenyl-β-lactams

• Benito Alcaide and
• Pedro Almendros

Beilstein J. Org. Chem. 2011, 7, 622–630, doi:10.3762/bjoc.7.73

• good yields for 2-azetidinones with n-butyl, THPOCH2, phenyl, and 2-naphthyl substituents. It should be mentioned that the cyclization of allenyl-β-lactams 1 is an application of the gold-catalyzed cycloisomerization of α-aminoallenes which was discovered earlier [32][33]. Although the mechanism of the

• was catalyzed by gold salts (AuCl3), allene cycloisomerization adducts 7 were obtained as the sole isomers (Scheme 3). The cyclization of allenyl-β-lactams 5 is an application of the previously reported gold-catalyzed cycloisomerization of α-hydroxyallenes [42][43][44]. Similarly to the transition

• -(2-alkynylphenyl)-β-lactams 18 has been accomplished (Scheme 10). Platinum was the metal of choice, gold salts being less effective [51]. This cycloisomerization can be viewed as a net intramolecular insertion of one end of the alkyne into the lactam amide bond with concurrent migration of the

A gold-catalyzed alkyne-diol cycloisomerization for the synthesis of oxygenated 5,5-spiroketals

• Sami F. Tlais and
• Gregory B. Dudley

Beilstein J. Org. Chem. 2011, 7, 570–577, doi:10.3762/bjoc.7.66

• cephalosporolides. Gold(I) chloride in methanol induced the cycloisomerization of a protected alkyne triol with concomitant deprotection to give a strategically hydroxylated 5,5-spiroketal, despite the potential for regiochemical complications and elimination to furan. Other late transition metal Lewis acids were

• less effective. The use of methanol as solvent helped suppress the formation of the undesired furan by-product. This study provides yet another example of the advantages of gold catalysis in the activation of alkyne π-systems. Keywords: alkynes; cyclocondensation; cycloisomerization; gold-catalyzed

• 5,5-spiroketals, including cyclocondensation of ketone diols [6][7], the cycloisomerization of alkyne diols (Scheme 1) [8][9][10][11][12][13][14][15][16], oxidative spirocyclization of tetrahydrofuryl propanols [17][18][19][20], and others. Cyclocondensation of ketone diols is perhaps the most

Gold catalysis for organic synthesis

• F. Dean Toste

Beilstein J. Org. Chem. 2011, 7, 553–554, doi:10.3762/bjoc.7.63

• , cycloaddition and cycloisomerization reactions, to applications in enantioselective catalysis, oxidative coupling and the total synthesis of natural products, and transformations of alkynes, allenes, alkenes and even C–H bonds. A true treasure chest of reactivity! I am grateful to all of the authors that have

Rh(I)-catalyzed intramolecular [2 + 2 + 1] cycloaddition of allenenes: Construction of bicyclo[4.3.0]nonenones with an angular methyl group and tricyclo[6.4.0.0^1,5]dodecenone

• Fuyuhiko Inagaki,
• Naoya Itoh,
• Yujiro Hayashi,
• Yumi Matsui and
• Chisato Mukai

Beilstein J. Org. Chem. 2011, 7, 404–409, doi:10.3762/bjoc.7.52

• , entries 3–5). Therefore, the formation of 12 must be rationalized by the Rh(I)-catalyzed cycloisomerization. The oxidative addition of the Rh(I)-catalyst to an alkene group and the distal double bond of the allenyl moiety would form a rhodabicyclo[4.3.0]nonene intermediate, which would collapse to the

Synthesis of fluorinated δ-lactams via cycloisomerization of gem-difluoropropargyl amides

• Satoru Arimitsu and
• Gerald B. Hammond

Beilstein J. Org. Chem. 2010, 6, No. 48, doi:10.3762/bjoc.6.48

• ; cycloisomerization; difluoropropargyl; enyne; ring-closing metathesis; Introduction It has been estimated that as many as 25% of all synthetic pharmaceutical drugs contain an amide bond [1]. Commonly, β- and γ-lactams are present in many natural products and pharmaceuticals, and the introduction of a gem

• (Scheme 3). In summary, gem-difluoro-1,7-enyne carbonyl derivatives are useful reaction partners in enyne metathesis cycloisomerization and CM–EYM tandem reactions catalyzed by ruthenium carbene complexes. The resulting diene products can be elaborated further using a Diels–Alder reaction. Comparison of

• fluorinated δ-lactams via cycloisomerization of gem-difluoropropargyl amides Acknowledgements We are grateful to the National Science Foundation for financial support (CHE-0809683) and to Professor Santos Fustero, Universidad de Valencia, Spain, for scientific cooperation and advice.

Recent progress on the total synthesis of acetogenins from Annonaceae

• Nianguang Li,
• Zhihao Shi,
• Yuping Tang,
• Jianwei Chen and
• Xiang Li

Beilstein J. Org. Chem. 2008, 4, No. 48, doi:10.3762/bjoc.4.48