Electrophilic olefin heterocyclization in organic synthesis. Stereoselective intramolecular amidomercuration of .GAMMA.-hydroxy-.DELTA.,.EPSILON.-unsaturated urethanes.
نویسندگان
چکیده
منابع مشابه
Electrophilic activation of unsaturated systems: Applications to selective organic synthesis*
Selected examples from previous work on iodonium-triggered approaches for the functionalization of unsaturated systems, which summarize innovative transformations, are presented. This section is mostly focused on C–C bond-forming processes from alkynes that are directly bonded to relevant heteroatoms, such as iodine, silicon, or sulfur. Besides, recent advances related to iodonium-promoted C–H ...
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Paniculatine 1, magnellanine 2. and magnellaninone 3 are three structurally similar tetracyclic alkaloids isolated and characterized by Castillo in 1976.3 Despite their unusual and interesting structures, there has been a paucity of effort directed toward the synthesis of this class of alkaloids.3 We report hem our studies on the synthesis and characterization of two tricyclic intermediates whi...
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در این پروژه ترکیبات 3-آریل-2h-بنزو[b]-4،1-اکسازین ها از مواد اولیه تجاری مشتقات دو آمینو فنول و ?-هالو کتون های آروماتیک در مایع یونی 1-اکتیل-3-متیل ایمیدازولیوم تترا فلورو بورات([omim]bf4) سنتز شده است. این واکنش توسط باز پتاسیم کربنات محلول از طریق o-آلکیلاسیون و سپس یک واکنش آمیداسیون درون مولکولی خود بخود در مدت زمان کوتاه انجام می شود. ترکیبات 4،1-بنزوکسازین به این روش با بهره خوب تا آلی ...
15 صفحه اولGold(I)-catalyzed stereoselective olefin cyclopropanation.
A triphenylphosphinegold(I)-catalyzed cyclopropanation of olefins using propargyl esters as gold(I)-carbene precursors is reported. This reaction provided the basis for the use of a DTBM-SEGPHOS gold(I) complex as a catalyst in the enantioselective (up to 94% ee) preparation of vinyl cyclopropanes with high cis-selectivity.
متن کاملasymmetric intramolecular olefin aminochlorination using chloride ion†
An iron-catalyzed enantioselective and diastereoselective intramolecular olefin aminochlorination reaction is reported (ee up to 92%, dr up to 15 : 1). In this reaction, a functionalized hydroxylamine and chloride ion are utilized as nitrogen and chlorine sources, respectively. This new method tolerates a range of synthetically valuable internal olefins that are all incompatible with existing a...
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ژورنال
عنوان ژورنال: Chemical and Pharmaceutical Bulletin
سال: 1989
ISSN: 0009-2363,1347-5223
DOI: 10.1248/cpb.37.2550