The first enantioselective biomimetic cyclization of polyprenoids

[1] ENZYMATIC CYCLIZATION OF SQUALENE AND OXIDOSQUALENE TO STEROLS AND TRITERPENES [J]. CHEMICAL REVIEWS, 1993, 93 (06) : 2189 - 2206

[2] Synthesis of decalin type chiral synthons based on enzymatic functionalisation and their application to the synthesis of (-)-ambrox and (+)-zonarol [J]. TETRAHEDRON-ASYMMETRY, 1998, 9 (10) : 1789 - 1799

[3] Synthesis of (+/-)-ambrox from (E)-nerolidol and beta-ionone via allylic alcohol [2,3] sigmatropic rearrangement [J]. JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (06) : 2215 - 2218

[4] BARTLETT PA, 1982, ASYMMETRIC SYNTHES B, V3, P390

[5] ENT-CHROMAZONAROL, A CHROMAN-SESQUITERPENOID FROM SPONGE DISIDEA-PALLESCENS [J]. EXPERIENTIA, 1975, 31 (10): : 1117 - 1118

[6] ENANTIOSELECTIVE TOTAL SYNTHESIS OF OLEANOLIC ACID, ERYTHRODIOL, BETA-AMYRIN, AND OTHER PENTACYCLIC TRITERPENES FROM A COMMON INTERMEDIATE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (19) : 8873 - 8874

[7] SOME METABOLITES OF THE MARINE SPONGES SMENOSPONGIA-AUREA AND SMENOSPONGIA (=POLYFIBROSPONGIA) ECHINA [J]. JOURNAL OF ORGANIC CHEMISTRY, 1980, 45 (08) : 1435 - 1441

[8] GAUSSIAN BASIS FUNCTIONS FOR USE IN MOLECULAR CALCULATIONS .1. CONTRACTION OF (9S5P) ATOMIC BASIS SETS FOR FIRST-ROW ATOMS [J]. JOURNAL OF CHEMICAL PHYSICS, 1970, 53 (07) : 2823 - +

[9] ZUR KENNTNIS DER TRITERPENE .190. EINE STEREOCHEMISCHE INTERPRETATION DER BIOGENETISCHEN ISOPRENREGEL BEI DEN TRITERPENEN [J]. HELVETICA CHIMICA ACTA, 1955, 38 (07) : 1890 - 1904

[10] CONFIGURATION-ODOR RELATIONSHIPS IN 5-BETA-AMBROX [J]. HELVETICA CHIMICA ACTA, 1990, 73 (07) : 1935 - 1947

[1] ENZYMATIC CYCLIZATION OF SQUALENE AND OXIDOSQUALENE TO STEROLS AND TRITERPENES [J]. CHEMICAL REVIEWS, 1993, 93 (06) : 2189 - 2206

[2] Synthesis of decalin type chiral synthons based on enzymatic functionalisation and their application to the synthesis of (-)-ambrox and (+)-zonarol [J]. TETRAHEDRON-ASYMMETRY, 1998, 9 (10) : 1789 - 1799

[3] Synthesis of (+/-)-ambrox from (E)-nerolidol and beta-ionone via allylic alcohol [2,3] sigmatropic rearrangement [J]. JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (06) : 2215 - 2218

[4] BARTLETT PA, 1982, ASYMMETRIC SYNTHES B, V3, P390

[5] ENT-CHROMAZONAROL, A CHROMAN-SESQUITERPENOID FROM SPONGE DISIDEA-PALLESCENS [J]. EXPERIENTIA, 1975, 31 (10): : 1117 - 1118

[6] ENANTIOSELECTIVE TOTAL SYNTHESIS OF OLEANOLIC ACID, ERYTHRODIOL, BETA-AMYRIN, AND OTHER PENTACYCLIC TRITERPENES FROM A COMMON INTERMEDIATE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (19) : 8873 - 8874

[7] SOME METABOLITES OF THE MARINE SPONGES SMENOSPONGIA-AUREA AND SMENOSPONGIA (=POLYFIBROSPONGIA) ECHINA [J]. JOURNAL OF ORGANIC CHEMISTRY, 1980, 45 (08) : 1435 - 1441

[8] GAUSSIAN BASIS FUNCTIONS FOR USE IN MOLECULAR CALCULATIONS .1. CONTRACTION OF (9S5P) ATOMIC BASIS SETS FOR FIRST-ROW ATOMS [J]. JOURNAL OF CHEMICAL PHYSICS, 1970, 53 (07) : 2823 - +

[9] ZUR KENNTNIS DER TRITERPENE .190. EINE STEREOCHEMISCHE INTERPRETATION DER BIOGENETISCHEN ISOPRENREGEL BEI DEN TRITERPENEN [J]. HELVETICA CHIMICA ACTA, 1955, 38 (07) : 1890 - 1904

[10] CONFIGURATION-ODOR RELATIONSHIPS IN 5-BETA-AMBROX [J]. HELVETICA CHIMICA ACTA, 1990, 73 (07) : 1935 - 1947