913255-79-5Relevant academic research and scientific papers
A three-step total synthesis of goniothalesdiol A using a one-pot Sharpless epoxidation/regioselective epoxide ring-opening
Ramesh, Perla,Reddy, Yarram Narasimha
supporting information, p. 1037 - 1039 (2017/03/31)
Using a one-pot Sharpless asymmetric epoxidation/regioselective epoxide ring-opening as a key step, the protecting-group-free total synthesis of goniothalesdiol A was accomplished in only three steps starting from commercially available trans-cinnamaldehy
A simple and efficient synthesis of goniothalesdiol A
Thakur, Pallavi,Boyapelly, Kumaraswamy,Gurram, Raji Reddy,Bandichhor, Rakeshwar,Mukkanti, Khagga
, p. 659 - 661 (2012/09/21)
A concise, simple, and efficient stereoselective total synthesis of goniothalesdiol A starting from commercially available 2-deoxy-d-ribose is described herein using a stereocontrolled Grignard reaction, olefin cross-metathesis, and oxy-Michael addition reactions as the key steps.
Tandem α-aminoxylation-allylation reaction based approach for the synthesis of goniothalesdiol A, leiocarpin A and (+)-goniodiol
Sabitha, Gowravaram,Rammohan Reddy,Yadav
, p. 6550 - 6553 (2012/01/06)
A short and efficient syntheses of goniothalesdiol A, leiocarpin A, and (+)-goniodiol are reported by a convergent strategy using tandem aminoxylation-allylation reaction as a key step starting from benzaldehyde.
Protecting-group-free total synthesis of goniothalesdiol A
Li, Junpeng,Zheng, Huaiji,Su, Yingpeng,Xie, Xingang,She, Xuegong
supporting information; experimental part, p. 2283 - 2284 (2010/11/03)
A concise asymmetric total synthesis of goniothalesdiol A was accomplished using protecting-group-free strategy, in which silyl-Prins cyclization was used as the key step. Georg Thieme Verlag Stuttgart - New York.
Stereoselective total synthesis of goniothalesdiol A via chiron approach
Yadav, Jhillu S.,Nageshwar Rao, Ragam,Somaiah, Ragam,Harikrishna, Valaboju,Subba Reddy, Basi V.
experimental part, p. 1362 - 1368 (2010/09/20)
The stereocontrolled synthesis of goniothalesdiol A, a dihydroxylated tetrahydropyran compound, has been accomplished using d-ribose as chiral precursor. The key steps involved are aryl Grignard reaction, stereoselective alkoxy-directed keto reduction, and intramolecular oxy-Michael addition.
First stereoselective total synthesis of Goniothalesdiol A
Yadav,Rami Reddy,Harikrishna,Subba Reddy
scheme or table, p. 1318 - 1320 (2009/06/28)
The first total synthesis of Goniothalesdiol A, isolated from the stems of Goniothalamus amuyon (Annonaceae) is reported. The C2 stereocentre and C3/C4 syn diol were created by a Sharpless kinetic resolution followed by acetonide formation. The tetrahydro
Asymmetric synthesis of Goniothalesdiol A from (R)-2,3-O-cyclohexylidine glyceraldehyde
Venkataiah, Mallam,Somaiah, Palabindela,Reddipalli, Gowrisankar,Fadnavis, Nitin W.
experimental part, p. 2230 - 2233 (2010/03/03)
Goniothalesdiol A 1 has been synthesized from (R)-2,3-O-cyclohexylidine glyceraldehyde with high stereoselectivity and 22% overall yield in 11 simple steps. The key features of the synthetic strategy include the stereocontrolled allylation of (R)-2,3-O-cy
