754188-59-5Relevant articles and documents
A novel, concise and efficient protocol for non-natural piperidine compounds
Chavan, Subhash P.,Dumare, Nilesh B.,Pawar, Kailash P.
, p. 32594 - 32598 (2014/08/18)
Formal synthesis of l-altro-1-deoxynojirimycin, cis-3-hydroxypipecolic acid along with synthesis of (R)-piperidinol and a conceptually different advanced intermediate for non-natural piperidine alkaloids is reported from cis-butene-1,4-diol. The key react
Stereoselective synthesis of microcarpalide
Ishigami, Ken,Watanabe, Hidenori,Kitahara, Takeshi
, p. 7546 - 7553 (2007/10/03)
Microcarpalide is a strong microfilament disrupting agent. The convergent and stereoselective synthesis of microcarpalide was succeeded via Julia olefination and macrolactonization.
Stereoselective synthesis of (-)-microcarpalide
Chavan, Subhash P.,Praveen, Cherukupally
, p. 1939 - 1941 (2007/10/03)
A highly convergent and efficient synthesis of (-)-microcarpalide, a 10-membered lactone displaying remarkable microfilament disrupting activity is described. Ring-closing metathesis and Sharpless asymmetric dihydroxylations are the key steps. Our strateg
An efficient stereoselective synthesis of (2S,4S,5R)-(-)- and (2R,4R,5S)-(+)-bulgecinine
Chavan, Subhash P.,Praveen, Cherukupally,Sharma, Pallavi,Kalkote
, p. 439 - 441 (2007/10/03)
A short synthetic route to (-)-and (+)-bulgecinine, the amino acid moiety of the bulgecins was achieved from the readily available nonchiral pool starting material cis-2-butene-1,4-diol employing a Claisen orthoester rearrangement and Sharpless asymmetric
A concise and stereoselective synthesis of (+)- and (-)-deoxoprosophylline
Chavan, Subhash P.,Praveen, Cherukupally
, p. 421 - 423 (2007/10/03)
An efficient synthesis of (+)- and (-)-deoxoprosophylline was accomplished from the readily available cis-2-butene-1,4-diol in which the Sharpless asymmetric dihydroxylation was used as the key step.
Synthesis of microcarpalide, a microfilament disrupting agent
Ishigami, Ken,Kitahara, Takeshi
, p. 785 - 790 (2007/10/03)
Microcarpalide is a strong microfilament disrupting agent. The convergent and stereoselective synthesis of microcarpalide was succeeded via Julia olefination and macrolactonization.
