نتایج جستجو برای: transannular interaction

تعداد نتایج: 565925  

Journal: :Organic letters 2013
Arthur J Catino Alexandra Sherlock Peyton Shieh Joseph S Wzorek David A Evans

Two transannular (TA) aldol reactions were used to assemble the tricyclic carbon skeleton found in the tigliane and daphnane classes of diterpene natural products.

2005
JOHN W. KIRKLIN

Fifteen of 194 patients (7.7%) with tetralogy of Fallot operated upon since January 1, 1972 under a protocol of routine primary repair despite young age died in-hospital. Most deaths were from low cardiac output. Young age and smallness of size increased the risk of operation. No deaths occurred among patients older than 4 years. High hematocrit was also a risk factor. Transannular patching has...

2013
Martin Zahel Peter Metz

(-)-Oxyphyllol was prepared in only 4 steps from an epoxy enone that already served as an intermediate for the total synthesis of the anticancer guaiane (-)-englerin A. A regio- and diastereoselective Co(II)-catalyzed hydration of the olefin and a transannular epoxide opening were used as the key reactions.

Journal: :Tetrahedron 2010
David B Freeman Alexandra A Holubec Matthew W Weiss Julie A Dixon Akio Kakefuda Masami Ohtsuka Munenori Inoue Rishi G Vaswani Hidenori Ohki Brian D Doan Sarah E Reisman Brian M Stoltz Joshua J Day Ran N Tao Noah A Dieterich John L Wood

Described is the construction of the N-methylwelwitindolinone C core via an efficient strategy that employs a sequential rhodium carbenoid-mediated O-H insertion, Claisen rearrangement and transannular [3+2] nitrone cycloaddition.

Journal: :Beilstein Journal of Organic Chemistry 2006
Grigoriy Sereda Jesse Van Heukelom Miles Koppang Sudha Ramreddy Nicole Collins

BACKGROUND Better understanding of the transannular influence of a substituent on the redox-potentials of bicyclo[2.2.2]octane-derived quinones will help in the design of new compounds with controlled biological activity. However, attempts to directly relate the reduction potentials of substituted triptycene-quinones to the electronic effects of substituents are often unsuccessful. RESULTS Fi...

Journal: :Journal of the American Chemical Society 2003
David A Evans Jeremy T Starr

An asymmetric synthesis of the cytotoxic natural product, (-)-FR182877 (1), has been achieved. Chirality for the entire structure was established using two (4R)-4-benzyl-2-oxazolidinone-mediated boron aldol reactions. A 19-membered macrocarbocycle was synthesized by the coupling of two fragments using a regioselective Suzuki coupling (17 + 23 --> 26; 84%) and macrocyclization of a beta-keto est...

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