19069-48-8Relevant articles and documents
Synthetic Studies on Arene-Olefin Cycloadditions: Total Synthesis of (+/-)-α-Cedrene
Wender, P. A.,Howbert, J. J.
, p. 688 - 690 (1981)
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Bang et al.
, p. 2087,2089,2090,2093 (1973)
Total synthesis of α-cedrene: A new strategy utilizing N- aziridinylimine radical chemistry
Lee, Hee-Yoon,Lee, Sejin,Kim, Deogil,Kim, Byung Kyu,Bahn, Jong Soo,Kim, Sunggak
, p. 7713 - 7716 (2007/10/03)
Tandem free radical cycloaddition reaction of the N-Aziridinylimine intermediate produced tricyclo[5.3.1.01,5]undecane skeleton stereoselectively. A total synthesis of α-cedrene was completed in three step sequence from the cyclization product.
THE DIRECT CONVERSION OF EPOXIDES INTO ALKENES via IODOHYDRINS BY in situ GENERATED HI
Garlaschelli, Luigi,Vidari, Giovanni
, p. 251 - 254 (2007/10/02)
Epoxides are easily converted into iodohydrins and alkenes are obtained from either epoxides or iodohydrins by treatment with HI, generated in situ from Ph3P*I2 in moist CH3CN.