TY - JOUR
T1 - Highly Enantioselective, Organocatalytic and Scalable Synthesis of a rare cis-cis-Tricyclic Diterpenoid
AU - Cobb, Alexander John Andre
AU - Townsend, Daniel
AU - Shankland, Kenneth
AU - Weymouth-Wilson, Alex
AU - Komsta, Zofia
AU - Evans, Tim
PY - 2020/3/18
Y1 - 2020/3/18
N2 - A highly enantioselective, organocatalytic and scalable synthesis of a very unusual cis-decalin-cis-hydrindane tricyclic diterpenoid system has been achieved. Despite the prevalent pharmacological space that the related trans-trans and trans-cis-systems occupy, there have been no reports of an asymmetric synthesis of the cis-cis systems in the literature until now. We demonstrate the flexibility of our approach not only through access to a diverse range of products, all of which are attained in exceptionally high selectivities, but also by showing their easy conversion to the corresponding trans-cis-system and other derivatives.
AB - A highly enantioselective, organocatalytic and scalable synthesis of a very unusual cis-decalin-cis-hydrindane tricyclic diterpenoid system has been achieved. Despite the prevalent pharmacological space that the related trans-trans and trans-cis-systems occupy, there have been no reports of an asymmetric synthesis of the cis-cis systems in the literature until now. We demonstrate the flexibility of our approach not only through access to a diverse range of products, all of which are attained in exceptionally high selectivities, but also by showing their easy conversion to the corresponding trans-cis-system and other derivatives.
KW - asymmetric synthesis
KW - decalin
KW - hydrindane
KW - organocatalysis
KW - terpenes
UR - http://www.scopus.com/inward/record.url?scp=85080142266&partnerID=8YFLogxK
U2 - 10.1002/chem.202000164
DO - 10.1002/chem.202000164
M3 - Article
SN - 0947-6539
VL - 26
SP - 3504
EP - 3508
JO - CHEMISTRY
JF - CHEMISTRY
IS - 16
ER -