N. N. Bhuvan Kumar

Mitsunobu and Related Reactions: Advances and Applications

10. Patented Literature 2616 10.1. Esterification 2616 10.2. Ether Formation 2619 10.2.1. Etherification without Cyclization 2619 10.2.2. Etherification with Cyclization 2624 10.3. N-Alkylation 2625 10.4. Other Reactions 2627 11. Summary and Outlook 2628 12. Note Added in Proof 2628 13. Abbreviations Used in This Review 2629 14. Acknowledgments 2629 15. Supporting Information Available 2630 16. References 2630

Rapid Photoassisted Access to N,O,S‐Polyheterocycles with Benzoazocine and Hydroquinoline Cores: Intramolecular Cycloadditions of Photogenerated Azaxylylenes

o-Azaxylylenes have been known for half a century,[1] but remained in relative synthetic obscurity until a decade ago, when in this journal Corey reported their first preparation under simple mild conditions via base-induced elimination of hydrogen chloride from derivatives of o-chloromethylaniline,[2] noting that “Surprisingly, simplest method possible for o-azaxylylene production [...] has never been reported.”

Reactivity of allenylphosphonates toward salicylaldehydes and activated phenols: facile synthesis of chromenes and substituted butadienes.

The reaction of salicylaldehydes with allenylphosphonates in the presence of a base leads to a variety of phosphono-chromenes and allylic phosphonates. Optimization of reaction conditions reveals that DBU (base) in DMSO (solvent) is the best combination in most cases, with DBU acting as an organocatalyst. PEG-400 also gave good results, but the yields were slightly lower than that in DMSO. Several of the key products have been characterized by single-crystal X-ray crystallography. Interconversion of E and Z isomers of phosphono-chromenes is demonstrated by (31)P NMR spectroscopy. A novel P-C bond cleavage reaction of some of these chromenes leading to substituted enones is also reported. In a few cases, phenol addition products are also isolated. In order to probe the pathways in the latter reaction, allenylphosphonates have also been treated with activated phenols in the presence of base to selectively afford either allylic phosphonyl ethers or vinylic phosphonyl ethers depending on the substituents on the allenylphosphonate. Theoretical calculations were consistent with experimental results. Finally, utilization of allylic phosphonyl ether in the Horner-Wadsworth-Emmons reaction to afford substituted trans-1,3-butadiene in good yields is demonstrated.

Cycloaddition Reactions of Allenylphosphonates and Related Allenes with Dialkyl Acetylenedicarboxylates, 1,3-Diphenylisobenzofuran, and Anthracene

Cycloaddition reactions of allenylphosphonates [(RO)(2)P(O)[(R(1))C═C═CR(2)(2)] with dialkyl acetylenedicarboxylates, 1,3-diphenylisobenzofuran, and anthracene have been investigated and compared with those of allenoates [(EtO(2)C)RC═C═CH(2)] and allenylphosphine oxides [Ph(2)P(O)(R(1))C═C═CR(2)(2)] in selected cases. Allenylphosphonates (RO)(2)P(O)(Ar)C═C═CH(2) with an α-aryl group preferentially undergo [4 + 2] cycloaddition with DMAD/DEAD under thermal activation, but in addition to the expected 1:1 (allene: DMAD) product, the reaction also leads to 1:2 as well as 2:1 products that were not reported before. When an extra vinyl group is present at the γ-carbon of allenylphosphonate [e.g., (OCH(2)CMe(2)CH(2)O)P(O)(Ph)C═C═CH(C═CHMe)], [4 + 2] cycloaddition takes place utilizing either the vinylic or the aryl end, but additionally a novel cyclization wherein complete opening of the [β,γ] carbon-carbon double bond of the allene is realized. In contrast to these, the reaction of allenylphosphonate (OCH(2)CMe(2)CH(2)O)P(O)(H)C═C═CMe(2) possessing a terminal ═CMe(2) group with DMAD occurs by both [2 + 2] cycloaddition and ene reaction. While the reaction of ═CH(2) terminal allenylphosphonates as well as allenylphosphine oxides with 1,3-diphenylisobenzofuran afforded preferentially endo-[4 + 2] cycloaddition products via [α,β] attack, the analogous allenoates [(EtO(2)C)RC═C═CH(2)] underwent exo-[4 + 2] cyclization. Under similar conditions, allenylphosphonates with a terminal ═CR(2) group gave only [β,γ]-cycloaddition products. An unusual ring-opening of a [4 + 2] cycloaddition product followed by ring-closing via [4 + 4] cycloaddition, as revealed by (31)P NMR spectroscopy, is reported. Anthracene reacted in a manner similar to 1,3-diphenylisobenzofuran, albeit with lower reactivity. Key products, including a set of exo- and endo- [4 + 2] cycloaddition products, have been characterized by single crystal X-ray crystallography.

Photoassisted Access to Enantiopure Conformationally Locked Ribofuranosylamines Spiro-Linked to Oxazolidino-Diketopiperazines.

N-Furoylated L-threonine-, serine-, or cysteine-based aminoacetals are coupled with o-aminoketones or aldehydes to offer rapid access to diverse enantiopure polyheterocycles possessing conformationally locked aminoglycoside-containing molecular scaffolds. The key step involves photogeneration of azaxylylenes which undergo [4 + 4] or [4 + 2] cycloadditions to the tethered furoyl pendants.

Intramolecular cycloadditions of photogenerated azaxylylenes with oxadiazoles provide direct access to versatile polyheterocyclic ketopiperazines containing a spiro-oxirane moiety.

Photogenerated azaxylylenes undergo intramolecular cycloadditions to 1,3,4-oxadiazole pendants, which are accompanied by concomitant release of dinitrogen, yielding functionalized ketopiperazinoquinolinols containing an oxirane moiety fused to the quinolinole moiety while spiro-connected to diketopiperazine. These primary photoproducts are reactive versatile intermediates which can be further derivatized under nucleophilic SN1- or SN2-like ring opening of the oxirane moiety. The oxidized quinolinones undergo new rearrangements under the conditions of the Schmidt reaction, leading to unprecedented triazacanoindolinones.

Structure and reactivity of tautomeric forms of zwitterionic species from the reaction of phosphorus(III) compounds with electron deficient alkenes and alkynes

Synthesis and reactivity of tautomeric forms of the zwitterions proposed in the phosphine catalysed transformations of electron-deficient alkenes/alkynes using the heterocycles [(t-BuNH)PN-t-Bu]2 (1) and Ph2P(NH-t-Bu) (2) are discussed. Thus, compounds (t-BuNH)P(N-t-Bu)2P(N-t-Bu)CHCH(CO2Me) (3), (t-BuNH)P(N-t-Bu)2P(N-t-Bu)CH2CH2(CN) (4) and Ph2P(N-t-Bu){C(Ph)CH(CO2Et)} (5) are isolated. A novel heterocycle [(t-BuNH)P(N-t-Bu)2P[C(CO2Me)–CH(OMe)–C(O)–N(t-Bu)–] (6) obtained by utilizing 1 and MeO2CCCCO2Me is described. The structural proof for the second stage intermediate after the addition of phenols/carboxylic acids to the zwitterions formed in the reaction of electron deficient alkenes with PIII compounds [e.g. {(t-BuNH)P(N-t-Bu)2P(NH-t-Bu)CH2CH2(CN)}+{X}− where X = PhO− + PhOH (7·Ph–O–H⋯OPh), 4-NO2–C6H4–CO2− + H2O (8·H2O)] is also provided for the first time. X-Ray structural characterisation of 3–8 has also been accomplished.

Intramolecular cycloadditions of photogenerated azaxylylenes: an experimental and theoretical study.

The mechanism of intramolecular cycloadditions of azaxylylenes photogenerated via excited-state intramolecular proton transfer (ESIPT) in aromatic o-amido ketones and aldehydes bearing unsaturated functionalities was studied experimentally and computationally. In time-correlated single-photon counting experiments, no relation was found between lifetimes of singlet species and the nature of the amide pendant, either unsaturated furanpropanamide, capable of photocyclization, or the acetamide control. Steady-state emission for amido-tetralone derivatives showed comparable dual emission bands, but bromo substitution decreased the intensity of the ESIPT band. The most reactive derivatives of amidobenzaldehydes were virtually lacking the ESIPT band. The quantum yield of cycloaddition is decreased in the presence of triplet quenchers, O2 or trans-piperylene, and improved with heavy atom substitution in the aromatic ring, providing further evidence for the initial mechanistic hypothesis in which the fast singlet-state ESIPT is accompanied by the ISC in the tautomer (azaxylylene), which undergoes stepwise addition to the tethered unsaturated pendants.

Photoassisted Diversity-Oriented Synthesis: Accessing 2,6-Epoxyazocane (Oxamorphan) Cores

The modular synthesis of photoprecursors and their photoinduced cyclization into substituted 1-benzazocanes of two distinct topologies is described. The key step producing an extended polyheterocyclic system involves the photogeneration of azaxylylenes and their subsequent intramolecular cycloaddition with furan-containing pendants tethered either via the aniline nitrogen or through the carbonyl group containing arm. The primary photoproducts—secondary or tertiary anilines which are not acylated at the nitrogen atom—undergo facile acid-catalyzed or spontaneous ring-opening–ring-closing rearrangement to yield fused polyheterocyclic structures possessing a 2,6-epoxyazocane (or oxamorphan) core.

Photoinduced Cycloadditions in the Diversity-Oriented Synthesis Toolbox: Increasing Complexity with Straightforward Post-Photochemical Modifications

Rapid growth of complexity and unprecedented molecular architectures are realized via the excited-state intramolecular proton transfer (ESIPT) in o-acylamidobenzaldehydes and ketones followed by [4+2] or [4+4] cycloadditions with subsequent postphotochemical modifications. The approach is congruent with Diversity-Oriented Synthesis: photoprecursors are synthesized in a modular fashion allowing for up to four diversity inputs. The complexity of the primary photoproducts is further enhanced using straightforward and high-yielding postphotochemical modification steps such as reactions with nitrile oxides, nitrones, Povarov reaction, and oxa-Diels-Alder reaction.