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[reaction: see text] A study of new nucleophilic addition/ring-closure (NARC) sequences has resulted in the development of a stereoselective synthetic route to 3-deoxy-8-oxatropanes. The new sequences consisted of either a syn or anti aldol addition, employing an omega-alkenoyl sultam, followed by two-step bicyclic ring construction involving, consecutively, ring-closing metathesis and intramolecular oxymercuration.  相似文献   
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We consider the problem of cotangent bundle reduction for proper non-free group actions at zero momentum. We show that in this context the symplectic stratification obtained by Sjamaar and Lerman refines in two ways: (i) each symplectic stratum admits a stratification which we call the secondary stratification with two distinct types of pieces, one of which is open and dense and symplectomorphic to a cotangent bundle; (ii) the reduced space at zero momentum admits a finer stratification than the symplectic one into pieces that are coisotropic in their respective symplectic strata.  相似文献   
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For the cotangent bundle TQ of a smooth Riemannian manifold acted upon by the lift of a smooth and proper action by isometries of a Lie group, we characterize the symplectic normal space at any point. We show that this space splits as the direct sum of the cotangent bundle of a linear space and a symplectic linear space coming from reduction of a coadjoint orbit. This characterization of the symplectic normal space can be expressed solely in terms of the group action on the base manifold and the coadjoint representation. Some relevant particular cases are explored.  相似文献   
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We show that, in terms of both implication and consistency strength, an extendible with a larger strong cardinal is stronger than an enhanced supercompact, which is itself stronger than a hypercompact, which is itself weaker than an extendible. All of these are easily seen to be stronger than a supercompact. We also study Cn‐supercompactness.  相似文献   
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Hybrid peptides consisting of alpha-amino acids with judiciously placed beta-amino acids show great promise as peptidomimetics in an increasing range of therapeutic applications. This reflects a combination of increased stability, high specificity and relative ease of synthesis.  相似文献   
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